BRCA1: Perbedaan antara revisi
Konten dihapus Konten ditambahkan
Fabi Fuu 76 (bicara | kontrib) Tidak ada ringkasan suntingan |
Fabi Fuu 76 (bicara | kontrib) Tag: Suntingan visualeditor-wikitext |
||
| (29 revisi perantara oleh pengguna yang sama tidak ditampilkan) | |||
Baris 2:
{{Infobox_gene}}
'''Breast cancer type 1 susceptibility protein''' adalah [[protein]] yang pada manusia dikodekan oleh [[gen]] '''''BRCA1'''.'' ''BRCA1'' adalah gen penekan tumor (''tumor supressor'') pada manusia dan bertanggung jawab untuk memperbaiki kerusakan DNA.<ref name=":0">{{Cite journal|last=Yoshida|first=Kiyotsugu|last2=Miki|first2=Yoshio|date=2004-11|title=Role of BRCA1 and BRCA2 as regulators of DNA repair, transcription, and cell cycle in response to DNA damage|url=https://onlinelibrary.wiley.com/doi/10.1111/j.1349-7006.2004.tb02195.x|journal=Cancer Science|language=en|volume=95|issue=11|pages=866–871|doi=10.1111/j.1349-7006.2004.tb02195.x|issn=1347-9032}}</ref><ref>{{Cite journal|last=Duncan|first=J. A.|last2=Reeves|first2=J. R.|last3=Cooke|first3=T. G.|date=1998-10-01|title=BRCA1 and BRCA2 proteins: roles in health and disease|url=https://mp.bmj.com/lookup/doi/10.1136/mp.51.5.237|journal=Molecular Pathology|language=en|volume=51|issue=5|pages=237–247|doi=10.1136/mp.51.5.237|issn=1366-8714|pmc=PMC395646|pmid=10193517}}</ref> [[Homologi sekuens|Ortolog]] dari gen ini umum ditemukan pada spesies [[vertebrata]] lain selain manusia, sedangkan [[genom]] [[invertebrata]] mengkodekan gen terkait yang berkerabat jauh.<ref name=":3">{{Cite web|title=BRCA1 orthologs|url=https://www.ncbi.nlm.nih.gov/gene/672/ortholog/|website=NCBI|language=en|access-date=2024-03-18}}</ref>
BRCA1 dan BRCA2 adalah protein yang tidak saling berhubungan,<ref>{{Cite journal|last=Irminger-Finger|first=Irmgard|last2=Ratajska|first2=Magda|last3=Pilyugin|first3=Maxim|date=2016-03|title=New concepts on BARD1: Regulator of BRCA pathways and beyond|url=https://linkinghub.elsevier.com/retrieve/pii/S1357272515300807|journal=The International Journal of Biochemistry & Cell Biology|language=en|volume=72|pages=1–17|doi=10.1016/j.biocel.2015.12.008}}</ref> tetapi keduanya biasanya diekspresikan dalam sel payudara dan jaringan lain, di mana mereka membantu memperbaiki DNA yang rusak, atau menghancurkan sel jika DNA tidak dapat diperbaiki.<ref name=":1">{{Cite book|last=Casaubon|first=Jesse T.|last2=Kashyap|first2=Sarang|last3=Regan|first3=John-Paul|date=2024|url=http://www.ncbi.nlm.nih.gov/books/NBK470239/|title=BRCA1 and BRCA2 Mutations|location=Treasure Island (FL)|publisher=StatPearls Publishing|pmid=29262038}}</ref><ref name=":0" /> Keduanya terlibat dalam perbaikan kerusakan [[kromosom]] dengan peran penting dalam perbaikan kerusakan untai ganda DNA.<ref name=":2">{{Cite journal|last=Friedenson|first=Bernard|date=2007-12|title=The BRCA1/2 pathway prevents hematologic cancers in addition to breast and ovarian cancers|url=https://bmccancer.biomedcentral.com/articles/10.1186/1471-2407-7-152|journal=BMC Cancer|language=en|volume=7|issue=1|doi=10.1186/1471-2407-7-152|issn=1471-2407|pmc=PMC1959234|pmid=17683622}}</ref><ref name=":0" />
Baris 9:
BRCA1 berasosiasi dengan protein penekan tumor lainnya, protein sensor kerusakan DNA, dan transduser sinyal untuk membentuk kompleks protein multi-subunit besar yang dikenal sebagai kompleks pengawasan genom yang terasosiasi dengan BRCA1 (''BRCA1-associated genome surveillance complex,'' BASC).<ref>{{Cite journal|last=Wang|first=Y.|last2=Cortez|first2=D.|last3=Yazdi|first3=P.|last4=Neff|first4=N.|last5=Elledge|first5=S. J.|last6=Qin|first6=J.|date=2000-04-15|title=BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures|url=https://pubmed.ncbi.nlm.nih.gov/10783165/|journal=Genes & Development|volume=14|issue=8|pages=927–939|issn=0890-9369|pmid=10783165}}</ref> Protein BRCA1 berasosiasi dengan RNA polimerase II, dan melalui domain C-terminal, juga berinteraksi dengan kompleks histone deacetylase.<ref name=":2" /> Dengan demikian, protein ini berperan dalam transkripsi, dan perbaikan DNA dari kerusakan DNA untai ganda ubiquitinasi, regulasi transkripsi, serta fungsi lainnya.<ref>{{Cite journal|last=Starita|first=L|date=2003-06|title=The multiple nuclear functions of BRCA1: transcription, ubiquitination and DNA repair|url=https://linkinghub.elsevier.com/retrieve/pii/S0955067403000425|journal=Current Opinion in Cell Biology|language=en|volume=15|issue=3|pages=345–350|doi=10.1016/S0955-0674(03)00042-5}}</ref>
== Penemuan ==
Bukti pertama keberadaan gen yang mengkode enzim perbaikan DNA yang terlibat dalam risiko terjadinya kanker payudara dikemukakan oleh laboratorium Mary-Claire King di UC Berkeley pada tahun 1990.<ref>{{Cite journal|last=Hall|first=Jeff M.|last2=Lee|first2=Ming K.|last3=Newman|first3=Beth|last4=Morrow|first4=Jan E.|last5=Anderson|first5=Lee A.|last6=Huey|first6=Bing|last7=King|first7=Mary-Claire|date=1990-12-21|title=Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21|url=https://www.science.org/doi/10.1126/science.2270482|journal=Science|language=en|volume=250|issue=4988|pages=1684–1689|doi=10.1126/science.2270482|issn=0036-8075}}</ref> Empat tahun kemudian, setelah terjadi perlombaan internasional untuk menemukannya,<ref>{{Cite news|last=Arney|first=Kat|date=2012-02-28|title=Tracking down the BRCA1 gene|url=https://news.cancerresearchuk.org/2012/02/28/high-impact-science-tracking-down-the-brca-genes-part-1/|newspaper=Cancer Research UK - Cancer News|language=en-GB|access-date=2024-03-18}}</ref> gen tersebut dikloning pada tahun 1994 oleh para ilmuwan di University of Utah, National Institute of Environmental Health Sciences (NIEHS), dan Myriad Genetics.<ref>{{Cite journal|last=Miki|first=Yoshio|last2=Swensen|first2=Jeff|last3=Shattuck-Eidens|first3=Donna|last4=Futreal|first4=P. Andrew|last5=Harshman|first5=Keith|last6=Tavtigian|first6=Sean|last7=Liu|first7=Qingyun|last8=Cochran|first8=Charles|last9=Bennett|first9=L. Michelle|date=1994-10-07|title=A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1|url=https://www.science.org/doi/10.1126/science.7545954|journal=Science|language=en|volume=266|issue=5182|pages=66–71|doi=10.1126/science.7545954|issn=0036-8075}}</ref>
== Lokasi gen ==
Gen BRCA1 manusia terletak pada lengan panjang (q) kromosom 17 di wilayah 2 pita 1, dari pasangan basa 41.196.312 hingga pasangan basa 41.277.500 (Build GRCh37 / HG19).<ref>{{Cite web|title=BRCA1 BRCA1 DNA repair associated [Homo sapiens (human)] - Gene - NCBI|url=https://www.ncbi.nlm.nih.gov/gene/672/|website=National Center for Biotechnology Information, U.S. National Library of Medicine|access-date=2024-03-18}}</ref> Ortolog BRCA1 telah diidentifikasi pada sebagian besar vertebrata yang memiliki data genom lengkap.<ref name=":3" />
== Fungsi dan mekanisme ==
BRCA1 adalah bagian dari kompleks protein yang berfungsi memperbaiki [[Perbaikan DNA|kerusakan untai ganda]] pada DNA. Ketika DNA mengalami kerusakan, untaian pada DNA tersebut akan terputus. Terkadang hanya satu untai yang putus, terkadang kedua untai putus secara bersamaan. Agen pengikat silang DNA (''DNA'' ''cross-linking agent'') adalah salah satu penyebab utama dari kerusakan kromosom dan DNA. Pemutusan untai ganda (''double strand breaks'') terjadi sebagai intermediet setelah ikatan silang ini dihilangkan. Mutasi bialelik pada ''BRCA1'' telah diidentifikasi bertanggung jawab atas [[Anemia Fanconi]], Complementation Group S (FA-S), penyakit genetik yang terkait dengan hipersensitivitas terhadap agen pengikat silang DNA.<ref>{{Cite journal|last=Sawyer|first=Sarah L.|last2=Tian|first2=Lei|last3=Kähkönen|first3=Marketta|last4=Schwartzentruber|first4=Jeremy|last5=Kircher|first5=Martin|last6=University of Washington Centre for Mendelian Genomics|last7=FORGE Canada Consortium|last8=Majewski|first8=Jacek|last9=Dyment|first9=David A.|date=2015-02-01|title=Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype|url=https://aacrjournals.org/cancerdiscovery/article/5/2/135/4638/Biallelic-Mutations-in-BRCA1-Cause-a-New-Fanconi|journal=Cancer Discovery|language=en|volume=5|issue=2|pages=135–142|doi=10.1158/2159-8290.CD-14-1156|issn=2159-8274|pmc=PMC4320660|pmid=25472942}}</ref>
[[Berkas:DsDNA break repair pathways.svg|jmpl|344x344px|Jenis-jenis perbaikan DNA untai ganda (''dsDNA repair'')]]
BRCA1 adalah bagian dari kompleks protein yang memperbaiki DNA ketika kedua untaiannya rusak. Ketika hal ini terjadi, sulit bagi mekanisme perbaikan untuk "mengetahui" cara mengganti urutan DNA yang benar. Ditambah lagi, terdapat berbagai mekanisme perbaikan DNA yang dapat dicoba. Mekanisme perbaikan untai ganda yang melibatkan BRCA1 adalah perbaikan yang diarahkan oleh homologi (''homology-directed repair''), di mana protein perbaikan menyalin urutan yang identik dari kromatid saudara (''sister chromatid'') yang masih utuh.<ref>{{Cite journal|last=Domchek|first=Susan M.|last2=Tang|first2=Jiangbo|last3=Stopfer|first3=Jill|last4=Lilli|first4=Dana R.|last5=Hamel|first5=Nancy|last6=Tischkowitz|first6=Marc|last7=Monteiro|first7=Alvaro N.A.|last8=Messick|first8=Troy E.|last9=Powers|first9=Jacquelyn|date=2013-04-01|title=Biallelic Deleterious BRCA1 Mutations in a Woman with Early-Onset Ovarian Cancer|url=https://aacrjournals.org/cancerdiscovery/article/3/4/399/4072/Biallelic-Deleterious-BRCA1-Mutations-in-a-Woman|journal=Cancer Discovery|language=en|volume=3|issue=4|pages=399–405|doi=10.1158/2159-8290.CD-12-0421|issn=2159-8274|pmc=PMC3625496|pmid=23269703}}</ref>
Di dalam nukleus dari berbagai jenis sel normal, protein BRCA1 berinteraksi dengan RAD51 selama perbaikan kerusakan untai ganda DNA.<ref>{{Cite journal|last=Boulton|first=S.J.|date=2006-10-01|title=Cellular functions of the BRCA tumour-suppressor proteins|url=https://portlandpress.com/biochemsoctrans/article/34/5/633/65958/Cellular-functions-of-the-BRCA-tumour-suppressor|journal=Biochemical Society Transactions|language=en|volume=34|issue=5|pages=633–645|doi=10.1042/BST0340633|issn=0300-5127}}</ref> Selain karena radiasi alami atau paparan yang lain, kerusakan ini dapat juga disebabkan ketika kromosom bertukar materi genetik, seperti pada proses rekombinasi homolog (contohnya, ''crossing over'' dalam pembelah meiosis). Protein BRCA2, yang memiliki fungsi yang mirip dengan BRCA1, juga berinteraksi dengan protein RAD51. Karena berperan dalam proses perbaikan kerusakan DNA, ketiga protein ini berperan penting dalam menjaga stabilitas genom manusia.<ref>{{Cite journal|last=Roy|first=Rohini|last2=Chun|first2=Jarin|last3=Powell|first3=Simon N.|date=2012-01|title=BRCA1 and BRCA2: different roles in a common pathway of genome protection|url=https://www.nature.com/articles/nrc3181|journal=Nature Reviews Cancer|language=en|volume=12|issue=1|pages=68–78|doi=10.1038/nrc3181|issn=1474-175X|pmc=PMC4972490|pmid=22193408}}</ref>
[[Berkas:Non homologous end joining and microhomology mediated end joining.png|kiri|jmpl|415x415px|''Non homogous end joining'' (NHEJ)]]
BRCA1 juga terlibat dalam jenis perbaikan DNA lainnya, yang disebut perbaikan ''mismatch''. BRCA1 berinteraksi dengan protein perbaikan ''mismatch'' DNA MSH2.<ref>{{Cite journal|last=Wang|first=Qiang|last2=Zhang|first2=Hongtao|last3=Guerrette|first3=Shawn|last4=Chen|first4=Jinqiu|last5=Mazurek|first5=Anthony|last6=Wilson|first6=Teresa|last7=Slupianek|first7=Artur|last8=Skorski|first8=Tomasz|last9=Fishel|first9=Richard|date=2001-08-02|title=Adenosine nucleotide modulates the physical interaction between hMSH2 and BRCA1|url=https://www.nature.com/articles/1204625|journal=Oncogene|language=en|volume=20|issue=34|pages=4640–4649|doi=10.1038/sj.onc.1204625|issn=0950-9232}}</ref> Eksperesi MSH2, MSH6, PARP, dan beberapa protein lain yang terlibat dalam perbaikan untai tunggal diketahui meningkat pada tumor payudara yang memiliki defisiensi BRCA1.<ref>{{Cite journal|last=Warmoes|first=Marc|last2=Jaspers|first2=Janneke E.|last3=Pham|first3=Thang V.|last4=Piersma|first4=Sander R.|last5=Oudgenoeg|first5=Gideon|last6=Massink|first6=Maarten P.G.|last7=Waisfisz|first7=Quinten|last8=Rottenberg|first8=Sven|last9=Boven|first9=Epie|date=2012-07|title=Proteomics of Mouse BRCA1-deficient Mammary Tumors Identifies DNA Repair Proteins with Potential Diagnostic and Prognostic Value in Human Breast Cancer|url=https://linkinghub.elsevier.com/retrieve/pii/S1535947620330061|journal=Molecular & Cellular Proteomics|language=en|volume=11|issue=7|pages=M111.013334–1–M111.013334-19|doi=10.1074/mcp.M111.013334|pmc=PMC3394939|pmid=22366898}}</ref>
BRCA1 dapat secara langsung berikatan dengan DNA, dengan afinitas yang lebih tinggi untuk struktur DNA yang bercabang (''branched structure''). Kemampuan untuk mengikat DNA ini berperan pada kemampuan BRCA1 dalam menghambat aktivitas nuklease kompleks MRN, juga aktivitas nuklease Mre11.<ref>{{Cite journal|last=Paull|first=Tanya T.|last2=Cortez|first2=David|last3=Bowers|first3=Blair|last4=Elledge|first4=Stephen J.|last5=Gellert|first5=Martin|date=2001-05-22|title=Direct DNA binding by Brca1|url=https://pnas.org/doi/full/10.1073/pnas.111125998|journal=Proceedings of the National Academy of Sciences|language=en|volume=98|issue=11|pages=6086–6091|doi=10.1073/pnas.111125998|issn=0027-8424|pmc=PMC33426|pmid=11353843}}</ref> Hal ini dapat menjelaskan peran BRCA1 untuk memfasilitasi perbaikan DNA dengan ketepatan yang lebih rendah melalui penggabungan ujung non-homolog (''non-homologous end joining'', NHEJ).<ref>{{Cite journal|last=Durant|first=Stephen T.|last2=Nickoloff|first2=Jac A|date=2005-09-22|title=Good Timing in the Cell Cycle for Precise DNA Repair by BRCA1|url=https://www.tandfonline.com/doi/full/10.4161/cc.4.9.2027|journal=Cell Cycle|language=en|volume=4|issue=9|pages=1216–1222|doi=10.4161/cc.4.9.2027|issn=1538-4101}}</ref> BRCA1 juga berkolokalisasi dengan γ-H2AX (histon H2AX terfosforilasi pada serine-139) dalam perbaikan kerusakan untai ganda DNA, yang mengindikasikan bahwa BRCA1 juga berperan dalam merekrut faktor-faktor perbaikan DNA.<ref>{{Cite journal|last=Starita|first=L|date=2003-06|title=The multiple nuclear functions of BRCA1: transcription, ubiquitination and DNA repair|url=https://linkinghub.elsevier.com/retrieve/pii/S0955067403000425|journal=Current Opinion in Cell Biology|language=en|volume=15|issue=3|pages=345–350|doi=10.1016/S0955-0674(03)00042-5}}</ref>
== Ekspresi ''BRCA1'' yang rendah pada kanker payudara ==
[[Berkas:Breast cancer ductal carcinoma in situ.jpg|jmpl|Kanker payudara berjenis duktal karsinoma ''in situ'']]
Ekspresi ''BRCA1'' berkurang atau tidak terdeteksi pada sebagian besar kanker payudara duktal tingkat tinggi (''high grade ductal breast cancers'').<ref>{{Cite journal|last=Wilson|first=Cindy A.|last2=Ramos|first2=Lillian|last3=Villaseñor|first3=Maria R.|last4=Anders|first4=Karl H.|last5=Press|first5=Michael F.|last6=Clarke|first6=Kathy|last7=Karlan|first7=Beth|last8=Chen|first8=Jun-Jie|last9=Scully|first9=Ralph|date=1999-02|title=Localization of human BRCA1 and its loss in high-grade, non-inherited breast carcinomas|url=https://www.nature.com/articles/ng0299_236|journal=Nature Genetics|language=en|volume=21|issue=2|pages=236–240|doi=10.1038/6029|issn=1061-4036}}</ref> Telah lama diketahui bahwa hilangnya aktivitas BRCA1, baik karena mutasi ''germ-line'' maupun karena penurunan regulasi ekspresi gen, menyebabkan pembentukan tumor pada jaringan-jaringan tertentu. Secara khusus, penurunan ekspresi ''BRCA1'' berkontribusi pada perkembangan tumor payudara sporadis (tidak diwariskan, terjadi secara spontan) dan yang diwariskan.<ref>{{Cite journal|last=Mueller|first=Christopher R|last2=Roskelley|first2=Calvin D|date=2002-02|title=Regulation of BRCA1 expression and its relationship to sporadic breast cancer|url=http://breast-cancer-research.biomedcentral.com/articles/10.1186/bcr557|journal=Breast Cancer Research|language=en|volume=5|issue=1|doi=10.1186/bcr557|issn=1465-542X|pmc=PMC154136|pmid=12559046}}</ref> Ekspresi ''BRCA1'' yang menurun bersifat tumorigenik, karena penurunan ekspresi ini memaikan peran penting dalam perbaikan kerusakan DNA, terutama pemutusan untai ganda, melalui jalur rekombinasi homolog yang berpotensi bebas dari kesalahan.<ref name=":4">{{Cite journal|last=Jacinto|first=F. V.|last2=Esteller|first2=M.|date=2007-07-01|title=Mutator pathways unleashed by epigenetic silencing in human cancer|url=https://academic.oup.com/mutage/article-lookup/doi/10.1093/mutage/gem009|journal=Mutagenesis|language=en|volume=22|issue=4|pages=247–253|doi=10.1093/mutage/gem009|issn=0267-8357}}</ref> Karena sel yang kekurangan protein BRCA1 cenderung memperbaiki kerusakan DNA dengan mekanisme alternatif yang lebih rentan terhadap kesalahan, penurunan atau penonaktifan protein ini menghasilkan mutasi dan penataan ulang kromosom (''chromosomal rearrangemen)'' yang dapat menyebabkan progresi kanker payudara.<ref name=":4" />
== Interaksi Protein ==
BRCA1 telah terbukti berinteraksi dengan protein-protein berikut:
* [[Abl gene|ABL1]]<ref name="pmid12024016">{{cite journal | vauthors = Foray N, Marot D, Randrianarison V, Venezia ND, Picard D, Perricaudet M, Favaudon V, Jeggo P | title = Constitutive association of BRCA1 and c-Abl and its ATM-dependent disruption after irradiation | journal = Mol. Cell. Biol. | volume = 22 | issue = 12 | pages = 4020–32 | date = June 2002 | pmid = 12024016 | pmc = 133860 | doi = 10.1128/MCB.22.12.4020-4032.2002 }}</ref>
* [[AKT1]]<ref name="pmid10542266">{{cite journal | vauthors = Altiok S, Batt D, Altiok N, Papautsky A, Downward J, Roberts TM, Avraham H | title = Heregulin induces phosphorylation of BRCA1 through phosphatidylinositol 3-Kinase/AKT in breast cancer cells | journal = J. Biol. Chem. | volume = 274 | issue = 45 | pages = 32274–8 | date = November 1999 | pmid = 10542266 | doi = 10.1074/jbc.274.45.32274 | doi-access = free }}</ref><ref name="pmid19074868">{{cite journal | vauthors = Xiang T, Ohashi A, Huang Y, Pandita TK, Ludwig T, Powell SN, Yang Q | title = Negative Regulation of AKT Activation by BRCA1 | journal = Cancer Res. | volume = 68 | issue = 24 | pages = 10040–4 | date = December 2008 | pmid = 19074868 | pmc = 2605656 | doi = 10.1158/0008-5472.CAN-08-3009 }}</ref>
* [[Androgen receptor|AR]]<ref name="pmid11016951">{{cite journal | vauthors = Yeh S, Hu YC, Rahman M, Lin HK, Hsu CL, Ting HJ, Kang HY, Chang C | title = Increase of androgen-induced cell death and androgen receptor transactivation by BRCA1 in prostate cancer cells | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 97 | issue = 21 | pages = 11256–61 | date = October 2000 | pmid = 11016951 | pmc = 17187 | doi = 10.1073/pnas.190353897 | bibcode = 2000PNAS...9711256Y | doi-access = free }}</ref>
* [[Ataxia telangiectasia and Rad3 related|ATR]]<ref name=pmid10608806/><ref name=pmid11114888/><ref name="pmid11016625">{{cite journal|date=September 2000|title=Ataxia telangiectasia-related protein is involved in the phosphorylation of BRCA1 following deoxyribonucleic acid damage|journal=Cancer Res.|volume=60|issue=18|pages=5037–9|pmid=11016625|vauthors=Chen J}}</ref><ref name=pmid11278964/>
* [[Ataxia telangiectasia mutated|ATM]]<ref name="pmid10608806">{{cite journal | vauthors = Kim ST, Lim DS, Canman CE, Kastan MB | title = Substrate specificities and identification of putative substrates of ATM kinase family members | journal = J. Biol. Chem. | volume = 274 | issue = 53 | pages = 37538–43 | date = December 1999 | pmid = 10608806 | doi = 10.1074/jbc.274.53.37538 | doi-access = free }}</ref><ref name="pmid11114888">{{cite journal | vauthors = Tibbetts RS, Cortez D, Brumbaugh KM, Scully R, Livingston D, Elledge SJ, Abraham RT | title = Functional interactions between BRCA1 and the checkpoint kinase ATR during genotoxic stress | journal = Genes Dev. | volume = 14 | issue = 23 | pages = 2989–3002 | date = December 2000 | pmid = 11114888 | pmc = 317107 | doi = 10.1101/gad.851000 }}</ref><ref name="pmid11278964">{{cite journal | vauthors = Gatei M, Zhou BB, Hobson K, Scott S, Young D, Khanna KK | title = Ataxia telangiectasia mutated (ATM) kinase and ATM and Rad3 related kinase mediate phosphorylation of Brca1 at distinct and overlapping sites. In vivo assessment using phospho-specific antibodies | journal = J. Biol. Chem. | volume = 276 | issue = 20 | pages = 17276–80 | date = May 2001 | pmid = 11278964 | doi = 10.1074/jbc.M011681200 | doi-access = free }}</ref><ref name="pmid10866324">{{cite journal | vauthors = Gatei M, Scott SP, Filippovitch I, Soronika N, Lavin MF, Weber B, Khanna KK | title = Role for ATM in DNA damage-induced phosphorylation of BRCA1 | journal = Cancer Res. | volume = 60 | issue = 12 | pages = 3299–304 | date = June 2000 | pmid = 10866324 }}</ref>
* [[ATF1]]
* [[BACH1]]<ref name=pmid11301010/>
* [[BARD1]]<ref name="pmid11301010">{{cite journal | vauthors = Cantor SB, Bell DW, Ganesan S, Kass EM, Drapkin R, Grossman S, Wahrer DC, Sgroi DC, Lane WS, Haber DA, Livingston DM | title = BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function | journal = Cell | volume = 105 | issue = 1 | pages = 149–60 | date = April 2001 | pmid = 11301010 | doi = 10.1016/S0092-8674(01)00304-X | doi-access = free }}</ref>
* [[BRCA2]]<ref name="pmid11477095">{{cite journal | vauthors = Sarkisian CJ, Master SR, Huber LJ, Ha SI, Chodosh LA | title = Analysis of murine Brca2 reveals conservation of protein–protein interactions but differences in nuclear localization signals | journal = J. Biol. Chem. | volume = 276 | issue = 40 | pages = 37640–8 | date = October 2001 | pmid = 11477095 | doi = 10.1074/jbc.M106281200 | doi-access = free }}</ref>
* [[BRCC3]]
* [[BRE (gene)|BRE]]
* [[BRIP1]]<ref name="pmid15242590">{{cite journal | vauthors = Botuyan MV, Nominé Y, Yu X, Juranic N, Macura S, Chen J, Mer G | title = Structural basis of BACH1 phosphopeptide recognition by BRCA1 tandem BRCT domains | journal = Structure | volume = 12 | issue = 7 | pages = 1137–46 | date = July 2004 | pmid = 15242590 | pmc = 3652423 | doi = 10.1016/j.str.2004.06.002 }}</ref><ref name="pmid14576433">{{cite journal | vauthors = Yu X, Chini CC, He M, Mer G, Chen J | title = The BRCT domain is a phospho-protein binding domain | journal = Science | volume = 302 | issue = 5645 | pages = 639–42 | date = October 2003 | pmid = 14576433 | doi = 10.1126/science.1088753 | bibcode = 2003Sci...302..639Y | s2cid = 29407635 }}</ref><ref name="pmid15133502">{{cite journal | vauthors = Clapperton JA, Manke IA, Lowery DM, Ho T, Haire LF, Yaffe MB, Smerdon SJ | title = Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer | journal = Nature Structural & Molecular Biology | volume = 11 | issue = 6 | pages = 512–8 | date = June 2004 | pmid = 15133502 | doi = 10.1038/nsmb775 | s2cid = 7354915 }}</ref>
* [[C-jun]]
* [[CHEK2]]<ref name="pmid10724175">{{cite journal | vauthors = Lee JS, Collins KM, Brown AL, Lee CH, Chung JH | title = hCds1-mediated phosphorylation of BRCA1 regulates the DNA damage response | journal = Nature | volume = 404 | issue = 6774 | pages = 201–4 | date = March 2000 | pmid = 10724175 | doi = 10.1038/35004614 | bibcode = 2000Natur.404..201L | s2cid = 4345911 }}</ref><ref name="pmid18804494">{{cite journal | vauthors = Chabalier-Taste C, Racca C, Dozier C, Larminat F | title = BRCA1 is regulated by Chk2 in response to spindle damage | journal = Biochim. Biophys. Acta | volume = 1783 | issue = 12 | pages = 2223–33 | date = December 2008 | pmid = 18804494 | doi = 10.1016/j.bbamcr.2008.08.006 | doi-access = free }}</ref>
* [[CLSPN]]<ref name="pmid15096610">{{cite journal | vauthors = Lin SY, Li K, Stewart GS, Elledge SJ | title = Human Claspin works with BRCA1 to both positively and negatively regulate cell proliferation | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 101 | issue = 17 | pages = 6484–9 | date = April 2004 | pmid = 15096610 | pmc = 404071 | doi = 10.1073/pnas.0401847101 | bibcode = 2004PNAS..101.6484L | doi-access = free }}</ref>
* [[Cofactor of BRCA1|COBRA1]]<ref name="pmid11739404">{{cite journal | vauthors = Ye Q, Hu YF, Zhong H, Nye AC, Belmont AS, Li R | title = BRCA1-induced large-scale chromatin unfolding and allele-specific effects of cancer-predisposing mutations | journal = J. Cell Biol. | volume = 155 | issue = 6 | pages = 911–21 | date = December 2001 | pmid = 11739404 | pmc = 2150890 | doi = 10.1083/jcb.200108049 }}</ref>
* [[CREB-binding protein|CREBBP]]<ref name="pmid12700228">{{cite journal | vauthors = Benezra M, Chevallier N, Morrison DJ, MacLachlan TK, El-Deiry WS, Licht JD | title = BRCA1 augments transcription by the NF-kappaB transcription factor by binding to the Rel domain of the p65/RelA subunit | journal = J. Biol. Chem. | volume = 278 | issue = 29 | pages = 26333–41 | date = July 2003 | pmid = 12700228 | doi = 10.1074/jbc.M303076200 | doi-access = free }}</ref><ref name="pmid10655477">{{cite journal | vauthors = Pao GM, Janknecht R, Ruffner H, Hunter T, Verma IM | title = CBP/p300 interact with and function as transcriptional coactivators of BRCA1 | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 97 | issue = 3 | pages = 1020–5 | date = February 2000 | pmid = 10655477 | pmc = 15508 | doi = 10.1073/pnas.97.3.1020 | bibcode = 2000PNAS...97.1020P | doi-access = free }}</ref><ref name="pmid9926942">{{cite journal | vauthors = Chai YL, Cui J, Shao N, Shyam E, Reddy P, Rao VN | title = The second BRCT domain of BRCA1 proteins interacts with p53 and stimulates transcription from the p21WAF1/CIP1 promoter | journal = Oncogene | volume = 18 | issue = 1 | pages = 263–8 | date = January 1999 | pmid = 9926942 | doi = 10.1038/sj.onc.1202323 | doi-access = free }}</ref><ref name="pmid11782371">{{cite journal | vauthors = Fan S, Ma YX, Wang C, Yuan RQ, Meng Q, Wang JA, Erdos M, Goldberg ID, Webb P, Kushner PJ, Pestell RG, Rosen EM | title = p300 Modulates the BRCA1 inhibition of estrogen receptor activity | journal = Cancer Res. | volume = 62 | issue = 1 | pages = 141–51 | date = January 2002 | pmid = 11782371 }}</ref><ref name="pmid9443979">{{cite journal | vauthors = Neish AS, Anderson SF, Schlegel BP, Wei W, Parvin JD | title = Factors associated with the mammalian RNA polymerase II holoenzyme | journal = Nucleic Acids Res. | volume = 26 | issue = 3 | pages = 847–53 | date = February 1998 | pmid = 9443979 | pmc = 147327 | doi = 10.1093/nar/26.3.847 }}</ref>
* [[CSNK2B]]<ref name="pmid10403822">{{cite journal | vauthors = O'Brien KA, Lemke SJ, Cocke KS, Rao RN, Beckmann RP | title = Casein kinase 2 binds to and phosphorylates BRCA1 | journal = Biochem. Biophys. Res. Commun. | volume = 260 | issue = 3 | pages = 658–64 | date = July 1999 | pmid = 10403822 | doi = 10.1006/bbrc.1999.0892 }}</ref>
* [[CSTF2]]<ref name="pmid11257228">{{cite journal | vauthors = Kleiman FE, Manley JL | title = The BARD1-CstF-50 interaction links mRNA 3' end formation to DNA damage and tumor suppression | journal = Cell | volume = 104 | issue = 5 | pages = 743–53 | date = March 2001 | pmid = 11257228 | doi = 10.1016/S0092-8674(01)00270-7 | doi-access = free }}</ref><ref name="pmid10477523">{{cite journal | vauthors = Kleiman FE, Manley JL | title = Functional interaction of BRCA1-associated BARD1 with polyadenylation factor CstF-50 | journal = Science | volume = 285 | issue = 5433 | pages = 1576–9 | date = September 1999 | pmid = 10477523 | doi = 10.1126/science.285.5433.1576 }}</ref>
* [[Cyclin-dependent kinase 2|CDK2]]<ref name="pmid9244350">{{cite journal | vauthors = Wang H, Shao N, Ding QM, Cui J, Reddy ES, Rao VN | title = BRCA1 proteins are transported to the nucleus in the absence of serum and splice variants BRCA1a, BRCA1b are tyrosine phosphoproteins that associate with E2F, cyclins and cyclin dependent kinases | journal = Oncogene | volume = 15 | issue = 2 | pages = 143–57 | date = Jul 1997 | pmid = 9244350 | doi = 10.1038/sj.onc.1201252 | doi-access = free }}</ref><ref name="pmid8764100">{{cite journal | vauthors = Chen Y, Farmer AA, Chen CF, Jones DC, Chen PL, Lee WH | title = BRCA1 is a 220-kDa nuclear phosphoprotein that is expressed and phosphorylated in a cell cycle-dependent manner | journal = Cancer Res. | volume = 56 | issue = 14 | pages = 3168–72 | date = July 1996 | pmid = 8764100 }}</ref><ref name="pmid10373534">{{cite journal | vauthors = Ruffner H, Jiang W, Craig AG, Hunter T, Verma IM | title = BRCA1 is phosphorylated at serine 1497 in vivo at a cyclin-dependent kinase 2 phosphorylation site | journal = Mol. Cell. Biol. | volume = 19 | issue = 7 | pages = 4843–54 | date = July 1999 | pmid = 10373534 | pmc = 84283 | doi = 10.1128/MCB.19.7.4843}}</ref>
* [[DHX9]]<ref name="pmid12592385">{{cite journal | vauthors = Schlegel BP, Starita LM, Parvin JD | title = Overexpression of a protein fragment of RNA helicase A causes inhibition of endogenous BRCA1 function and defects in ploidy and cytokinesis in mammary epithelial cells | journal = Oncogene | volume = 22 | issue = 7 | pages = 983–91 | date = February 2003 | pmid = 12592385 | doi = 10.1038/sj.onc.1206195 | doi-access = free }}</ref><ref name="pmid9662397">{{cite journal | vauthors = Anderson SF, Schlegel BP, Nakajima T, Wolpin ES, Parvin JD | title = BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A | journal = Nat. Genet. | volume = 19 | issue = 3 | pages = 254–6 | date = July 1998 | pmid = 9662397 | doi = 10.1038/930 | s2cid = 10953768 }}</ref>
* [[ELK4]]<ref name="pmid11313879">{{cite journal | vauthors = Chai Y, Chipitsyna G, Cui J, Liao B, Liu S, Aysola K, Yezdani M, Reddy ES, Rao VN | title = c-Fos oncogene regulator Elk-1 interacts with BRCA1 splice variants BRCA1a/1b and enhances BRCA1a/1b-mediated growth suppression in breast cancer cells | journal = Oncogene | volume = 20 | issue = 11 | pages = 1357–67 | date = March 2001 | pmid = 11313879 | doi = 10.1038/sj.onc.1204256 | doi-access = free }}</ref>
* [[EP300]]<ref name=pmid10655477/><ref name=pmid11782371/>
* [[Estrogen receptor alpha|ESR1]]<ref name=pmid11782371/><ref name="pmid11493692">{{cite journal | vauthors = Zheng L, Annab LA, Afshari CA, Lee WH, Boyer TG | title = BRCA1 mediates ligand-independent transcriptional repression of the estrogen receptor | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 98 | issue = 17 | pages = 9587–92 | date = August 2001 | pmid = 11493692 | pmc = 55496 | doi = 10.1073/pnas.171174298 | bibcode = 2001PNAS...98.9587Z | doi-access = free }}</ref><ref name="pmid11244506">{{cite journal | vauthors = Fan S, Ma YX, Wang C, Yuan RQ, Meng Q, Wang JA, Erdos M, Goldberg ID, Webb P, Kushner PJ, Pestell RG, Rosen EM | title = Role of direct interaction in BRCA1 inhibition of estrogen receptor activity | journal = Oncogene | volume = 20 | issue = 1 | pages = 77–87 | date = January 2001 | pmid = 11244506 | doi = 10.1038/sj.onc.1204073 | doi-access = free }}</ref><ref name="pmid12400015">{{cite journal | vauthors = Kawai H, Li H, Chun P, Avraham S, Avraham HK | title = Direct interaction between BRCA1 and the estrogen receptor regulates vascular endothelial growth factor (VEGF) transcription and secretion in breast cancer cells | journal = Oncogene | volume = 21 | issue = 50 | pages = 7730–9 | date = October 2002 | pmid = 12400015 | doi = 10.1038/sj.onc.1205971 | doi-access = free }}</ref>
* [[FANCA]]<ref name="pmid12354784">{{cite journal | vauthors = Folias A, Matkovic M, Bruun D, Reid S, Hejna J, Grompe M, D'Andrea A, Moses R | title = BRCA1 interacts directly with the Fanconi anemia protein FANCA | journal = Hum. Mol. Genet. | volume = 11 | issue = 21 | pages = 2591–7 | date = October 2002 | pmid = 12354784 | doi = 10.1093/hmg/11.21.2591 | doi-access = free }}</ref>
* [[FANCD2]]<ref name="pmid14499622">{{cite journal | vauthors = Reuter TY, Medhurst AL, Waisfisz Q, Zhi Y, Herterich S, Hoehn H, Gross HJ, Joenje H, Hoatlin ME, Mathew CG, Huber PA | title = Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport | journal = Exp. Cell Res. | volume = 289 | issue = 2 | pages = 211–21 | date = October 2003 | pmid = 14499622 | doi = 10.1016/S0014-4827(03)00261-1 }}</ref>
* [[FHL2]]<ref name="pmid14550570">{{cite journal | vauthors = Yan J, Zhu J, Zhong H, Lu Q, Huang C, Ye Q | title = BRCA1 interacts with FHL2 and enhances FHL2 transactivation function | journal = FEBS Lett. | volume = 553 | issue = 1–2 | pages = 183–9 | date = October 2003 | pmid = 14550570 | doi = 10.1016/S0014-5793(03)00978-5 | s2cid = 31566004 | doi-access = free }}</ref><ref name="pmid14986435">{{cite journal | vauthors = Yan JH, Ye QN, Zhu JH, Zhong HJ, Zheng HY, Huang CF | title = [Isolation and characterization of a BRCA1-interacting protein] | language = zh | journal = Yi Chuan Xue Bao | volume = 30 | issue = 12 | pages = 1161–6 | date = December 2003 | pmid = 14986435 }}</ref>
* [[H2AFX]]<ref name="pmid10959836">{{cite journal | vauthors = Paull TT, Rogakou EP, Yamazaki V, Kirchgessner CU, Gellert M, Bonner WM | title = A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage | journal = Curr. Biol. | volume = 10 | issue = 15 | pages = 886–95 | year = 2000 | pmid = 10959836 | doi = 10.1016/S0960-9822(00)00610-2 | doi-access = free }}</ref>
* [[JUNB]]<ref name=pmid12080089/>
* [[JunD]]<ref name="pmid12080089">{{cite journal | vauthors = Hu YF, Li R | title = JunB potentiates function of BRCA1 activation domain 1 (AD1) through a coiled-coil-mediated interaction | journal = Genes Dev. | volume = 16 | issue = 12 | pages = 1509–17 | date = June 2002 | pmid = 12080089 | pmc = 186344 | doi = 10.1101/gad.995502 }}</ref>
* [[LMO4]]<ref name="pmid12925972">{{cite journal | vauthors = Sutherland KD, Visvader JE, Choong DY, Sum EY, Lindeman GJ, Campbell IG | title = Mutational analysis of the LMO4 gene, encoding a BRCA1-interacting protein, in breast carcinomas | journal = Int. J. Cancer | volume = 107 | issue = 1 | pages = 155–8 | date = October 2003 | pmid = 12925972 | doi = 10.1002/ijc.11343 | s2cid = 20908722 | doi-access = free }}</ref><ref name="pmid11751867">{{cite journal | vauthors = Sum EY, Peng B, Yu X, Chen J, Byrne J, Lindeman GJ, Visvader JE | title = The LIM domain protein LMO4 interacts with the cofactor CtIP and the tumor suppressor BRCA1 and inhibits BRCA1 activity | journal = J. Biol. Chem. | volume = 277 | issue = 10 | pages = 7849–56 | date = March 2002 | pmid = 11751867 | doi = 10.1074/jbc.M110603200 | doi-access = free }}</ref>
* [[MAP3K3]]<ref name="pmid15205325">{{cite journal | vauthors = Gilmore PM, McCabe N, Quinn JE, Kennedy RD, Gorski JJ, Andrews HN, McWilliams S, Carty M, Mullan PB, Duprex WP, Liu ET, Johnston PG, Harkin DP | title = BRCA1 interacts with and is required for paclitaxel-induced activation of mitogen-activated protein kinase kinase kinase 3 | journal = Cancer Res. | volume = 64 | issue = 12 | pages = 4148–54 | date = June 2004 | pmid = 15205325 | doi = 10.1158/0008-5472.CAN-03-4080 | doi-access = free }}</ref>
* [[MED1]]<ref name="pmid15208681">{{cite journal | vauthors = Wada O, Oishi H, Takada I, Yanagisawa J, Yano T, Kato S | title = BRCA1 function mediates a TRAP/DRIP complex through direct interaction with TRAP220 | journal = Oncogene | volume = 23 | issue = 35 | pages = 6000–5 | date = August 2004 | pmid = 15208681 | doi = 10.1038/sj.onc.1207786 | doi-access = free }}</ref>
* [[MED17]]<ref name="pmid11504724">{{cite journal | vauthors = Chiba N, Parvin JD | title = Redistribution of BRCA1 among four different protein complexes following replication blockage | journal = J. Biol. Chem. | volume = 276 | issue = 42 | pages = 38549–54 | date = October 2001 | pmid = 11504724 | doi = 10.1074/jbc.M105227200 | doi-access = free }}</ref><ref name=pmid15208681/><ref name="pmid12154023">{{cite journal | vauthors = Chiba N, Parvin JD | title = The BRCA1 and BARD1 association with the RNA polymerase II holoenzyme | journal = Cancer Res. | volume = 62 | issue = 15 | pages = 4222–8 | date = August 2002 | pmid = 12154023 }}</ref>
* [[MED21]]<ref name="pmid9159119">{{cite journal | vauthors = Scully R, Anderson SF, Chao DM, Wei W, Ye L, Young RA, Livingston DM, Parvin JD | title = BRCA1 is a component of the RNA polymerase II holoenzyme | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 94 | issue = 11 | pages = 5605–10 | date = May 1997 | pmid = 9159119 | pmc = 20825 | doi = 10.1073/pnas.94.11.5605 | bibcode = 1997PNAS...94.5605S | doi-access = free }}</ref>
* [[MED24]]<ref name=pmid15208681/>
* [[MRE11A]]<ref name=pmid10783165/><ref name=pmid11504724/><ref name=pmid10426999/><ref name="pmid11353843">{{cite journal | vauthors = Paull TT, Cortez D, Bowers B, Elledge SJ, Gellert M | title = Direct DNA binding by Brca1 | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 98 | issue = 11 | pages = 6086–91 | date = May 2001 | pmid = 11353843 | pmc = 33426 | doi = 10.1073/pnas.111125998 | doi-access = free }}</ref>
* [[MSH2]]<ref name="pmid10783165">{{cite journal | vauthors = Wang Y, Cortez D, Yazdi P, Neff N, Elledge SJ, Qin J | title = BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures | journal = Genes Dev. | volume = 14 | issue = 8 | pages = 927–39 | date = April 2000 | pmid = 10783165 | pmc = 316544 | doi = 10.1101/gad.14.8.927}}</ref>
* [[MSH3]]<ref name="pmid14578343">{{cite journal | vauthors = Rodriguez M, Yu X, Chen J, Songyang Z | title = Phosphopeptide binding specificities of BRCA1 COOH-terminal (BRCT) domains | journal = J. Biol. Chem. | volume = 278 | issue = 52 | pages = 52914–8 | date = December 2003 | pmid = 14578343 | doi = 10.1074/jbc.C300407200 | doi-access = free }}</ref>
* [[MSH6]]<ref name=pmid10783165/>
* [[Myc]]<ref name=pmid11916966/><ref name="pmid14612409">{{cite journal | vauthors = Xiong J, Fan S, Meng Q, Schramm L, Wang C, Bouzahza B, Zhou J, Zafonte B, Goldberg ID, Haddad BR, Pestell RG, Rosen EM | title = BRCA1 inhibition of telomerase activity in cultured cells | journal = Mol. Cell. Biol. | volume = 23 | issue = 23 | pages = 8668–90 | date = December 2003 | pmid = 14612409 | pmc = 262673 | doi = 10.1128/MCB.23.23.8668-8690.2003 }}</ref><ref name="pmid12646176">{{cite journal | vauthors = Zhou C, Liu J | title = Inhibition of human telomerase reverse transcriptase gene expression by BRCA1 in human ovarian cancer cells | journal = Biochem. Biophys. Res. Commun. | volume = 303 | issue = 1 | pages = 130–6 | date = March 2003 | pmid = 12646176 | doi = 10.1016/S0006-291X(03)00318-8 }}</ref>
* [[Nibrin|NBN]]<ref name=pmid10783165/><ref name=pmid11504724/><ref name=pmid10426999/>
* [[N-myc-interactor|NMI]]<ref name="pmid11916966">{{cite journal | vauthors = Li H, Lee TH, Avraham H | title = A novel tricomplex of BRCA1, Nmi, and c-Myc inhibits c-Myc-induced human telomerase reverse transcriptase gene (hTERT) promoter activity in breast cancer | journal = J. Biol. Chem. | volume = 277 | issue = 23 | pages = 20965–73 | date = June 2002 | pmid = 11916966 | doi = 10.1074/jbc.M112231200 | doi-access = free }}</ref>
* [[NPM1]]
* [[Nuclear receptor coactivator 2|NCOA2]]<ref name="pmid11085509">{{cite journal | vauthors = Park JJ, Irvine RA, Buchanan G, Koh SS, Park JM, Tilley WD, Stallcup MR, Press MF, Coetzee GA | title = Breast cancer susceptibility gene 1 (BRCAI) is a coactivator of the androgen receptor | journal = Cancer Res. | volume = 60 | issue = 21 | pages = 5946–9 | date = November 2000 | pmid = 11085509 }}</ref>
* [[NUFIP1]]<ref name="pmid15107825">{{cite journal | vauthors = Cabart P, Chew HK, Murphy S | title = BRCA1 cooperates with NUFIP and P-TEFb to activate transcription by RNA polymerase II | journal = Oncogene | volume = 23 | issue = 31 | pages = 5316–29 | date = July 2004 | pmid = 15107825 | doi = 10.1038/sj.onc.1207684 | doi-access = free }}</ref>
* [[P53]]<ref name=pmid9926942/><ref name="pmid14710355">{{cite journal | vauthors = Abramovitch S, Werner H | title = Functional and physical interactions between BRCA1 and p53 in transcriptional regulation of the IGF-IR gene | journal = Horm. Metab. Res. | volume = 35 | issue = 11–12 | pages = 758–62 | year = 2003 | pmid = 14710355 | doi = 10.1055/s-2004-814154 | s2cid = 20898175 }}</ref><ref name="pmid9482880">{{cite journal | vauthors = Ouchi T, Monteiro AN, August A, Aaronson SA, Hanafusa H | title = BRCA1 regulates p53-dependent gene expression | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 95 | issue = 5 | pages = 2302–6 | date = March 1998 | pmid = 9482880 | pmc = 19327 | doi = 10.1073/pnas.95.5.2302 | bibcode = 1998PNAS...95.2302O | doi-access = free }}</ref><ref name="pmid9582019">{{cite journal | vauthors = Zhang H, Somasundaram K, Peng Y, Tian H, Zhang H, Bi D, Weber BL, El-Deiry WS | title = BRCA1 physically associates with p53 and stimulates its transcriptional activity | journal = Oncogene | volume = 16 | issue = 13 | pages = 1713–21 | date = April 1998 | pmid = 9582019 | doi = 10.1038/sj.onc.1201932 | doi-access = free }}</ref>
* [[PALB2]]<ref name="pmid19369211">{{cite journal | vauthors = Sy SM, Huen MS, Chen J | title = PALB2 is an integral component of the BRCA complex required for homologous recombination repair | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 106 | issue = 17 | pages = 7155–60 | date = April 2009 | pmid = 19369211 | pmc = 2678481 | doi = 10.1073/pnas.0811159106 | bibcode = 2009PNAS..106.7155S | doi-access = free }}</ref>
* [[POLR2A]]<ref name=pmid11504724/><ref name=pmid9159119/><ref name="pmid14506230">{{cite journal | vauthors = Krum SA, Miranda GA, Lin C, Lane TF | title = BRCA1 associates with processive RNA polymerase II | journal = J. Biol. Chem. | volume = 278 | issue = 52 | pages = 52012–20 | date = December 2003 | pmid = 14506230 | doi = 10.1074/jbc.M308418200 | doi-access = free }}</ref><ref name="pmid12955082">{{cite journal | vauthors = Krum SA, Womack JE, Lane TF | title = Bovine BRCA1 shows classic responses to genotoxic stress but low in vitro transcriptional activation activity | journal = Oncogene | volume = 22 | issue = 38 | pages = 6032–44 | date = September 2003 | pmid = 12955082 | doi = 10.1038/sj.onc.1206515 | doi-access = free }}</ref>
* [[PPP1CA]]<ref name="pmid12438214">{{cite journal | vauthors = Liu Y, Virshup DM, White RL, Hsu LC | title = Regulation of BRCA1 phosphorylation by interaction with protein phosphatase 1alpha | journal = Cancer Res. | volume = 62 | issue = 22 | pages = 6357–61 | date = November 2002 | pmid = 12438214 }}</ref>
* [[Rad50]]<ref name=pmid10783165/><ref name=pmid11504724/><ref name="pmid10426999">{{cite journal | vauthors = Zhong Q, Chen CF, Li S, Chen Y, Wang CC, Xiao J, Chen PL, Sharp ZD, Lee WH | title = Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response | journal = Science | volume = 285 | issue = 5428 | pages = 747–50 | date = July 1999 | pmid = 10426999 | doi = 10.1126/science.285.5428.747 }}</ref>
* [[RAD51]]<ref name="pmid9774970">{{cite journal | vauthors = Chen J, Silver DP, Walpita D, Cantor SB, Gazdar AF, Tomlinson G, Couch FJ, Weber BL, Ashley T, Livingston DM, Scully R | title = Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells | journal = Mol. Cell | volume = 2 | issue = 3 | pages = 317–28 | date = September 1998 | pmid = 9774970 | doi = 10.1016/S1097-2765(00)80276-2 | doi-access = free }}</ref><ref name="pmid9008167">{{cite journal | vauthors = Scully R, Chen J, Plug A, Xiao Y, Weaver D, Feunteun J, Ashley T, Livingston DM | title = Association of BRCA1 with Rad51 in mitotic and meiotic cells | journal = Cell | volume = 88 | issue = 2 | pages = 265–75 | date = January 1997 | pmid = 9008167 | doi = 10.1016/S0092-8674(00)81847-4 | doi-access = free }}</ref>
* [[RBBP4]]
== Referensi ==
<references />
==External links==
{{Commons category|BRCA1}}
* {{MeshName|BRCA1+Protein|3=BRCA1 Protein}}
* {{MeshName|Genes,+BRCA1|3=Genes, BRCA1}}
* [https://www.ebi.ac.uk/pdbe/pdbe-kb/proteins/P38398 PDBe-KB] memberikan gambaran umum tentang semua informasi struktur yang tersedia dalam PDB untuk protein BRCA1 manusia.
[[Kategori: Gen penekan tumor]]
| |||