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BRCA1 and Its Network of Interacting Partners
BRCA1 is a large multi-domain protein with a pivotal role in maintaining genome stability and cell cycle progression. Germline mutations in the BRCA1 gene confer an estimated lifetime risk of 60%–80% for breast cancer and 15%–60% for ovarian cancer. Many of the germline mutations associated with can...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009870/ https://www.ncbi.nlm.nih.gov/pubmed/24832651 http://dx.doi.org/10.3390/biology2010040 |
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author | Christou, Charita M. Kyriacou, Kyriacos |
author_facet | Christou, Charita M. Kyriacou, Kyriacos |
author_sort | Christou, Charita M. |
collection | PubMed |
description | BRCA1 is a large multi-domain protein with a pivotal role in maintaining genome stability and cell cycle progression. Germline mutations in the BRCA1 gene confer an estimated lifetime risk of 60%–80% for breast cancer and 15%–60% for ovarian cancer. Many of the germline mutations associated with cancer development are concentrated in the amino terminal RING domain and the carboxyl terminal BRCT motifs of BRCA1, which are the most well-characterized regions of the protein. The function of BRCA1 in DNA repair, transcription and cell cycle control through the DNA damage response is orchestrated through its association with an impressive repertoire of protein complexes. The association of BRCA1 with ATM/ATR, CHK2 and Aurora A protein kinases regulates cell cycle progression, whilst its association with RAD51 has a direct impact on the repair of double strand DNA breaks (DSBs) by homologous recombination (HR). BRCA1 interactions with the MRN complex of proteins, with the BRCC complex of proteins that exhibit E3 ligase activity and with the phosphor proteins CtIP, BACH1 (BRIP1) and Abraxas (CCDC98) are also implicated in DNA repair mechanisms and cell cycle checkpoint control. BRCA1 through its association with specific proteins and multi-protein complexes is a sentinel of the normal cell cycle control and DNA repair. |
format | Online Article Text |
id | pubmed-4009870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40098702014-05-07 BRCA1 and Its Network of Interacting Partners Christou, Charita M. Kyriacou, Kyriacos Biology (Basel) Review BRCA1 is a large multi-domain protein with a pivotal role in maintaining genome stability and cell cycle progression. Germline mutations in the BRCA1 gene confer an estimated lifetime risk of 60%–80% for breast cancer and 15%–60% for ovarian cancer. Many of the germline mutations associated with cancer development are concentrated in the amino terminal RING domain and the carboxyl terminal BRCT motifs of BRCA1, which are the most well-characterized regions of the protein. The function of BRCA1 in DNA repair, transcription and cell cycle control through the DNA damage response is orchestrated through its association with an impressive repertoire of protein complexes. The association of BRCA1 with ATM/ATR, CHK2 and Aurora A protein kinases regulates cell cycle progression, whilst its association with RAD51 has a direct impact on the repair of double strand DNA breaks (DSBs) by homologous recombination (HR). BRCA1 interactions with the MRN complex of proteins, with the BRCC complex of proteins that exhibit E3 ligase activity and with the phosphor proteins CtIP, BACH1 (BRIP1) and Abraxas (CCDC98) are also implicated in DNA repair mechanisms and cell cycle checkpoint control. BRCA1 through its association with specific proteins and multi-protein complexes is a sentinel of the normal cell cycle control and DNA repair. MDPI 2012-12-31 /pmc/articles/PMC4009870/ /pubmed/24832651 http://dx.doi.org/10.3390/biology2010040 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Christou, Charita M. Kyriacou, Kyriacos BRCA1 and Its Network of Interacting Partners |
title | BRCA1 and Its Network of Interacting Partners |
title_full | BRCA1 and Its Network of Interacting Partners |
title_fullStr | BRCA1 and Its Network of Interacting Partners |
title_full_unstemmed | BRCA1 and Its Network of Interacting Partners |
title_short | BRCA1 and Its Network of Interacting Partners |
title_sort | brca1 and its network of interacting partners |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009870/ https://www.ncbi.nlm.nih.gov/pubmed/24832651 http://dx.doi.org/10.3390/biology2010040 |
work_keys_str_mv | AT christoucharitam brca1anditsnetworkofinteractingpartners AT kyriacoukyriacos brca1anditsnetworkofinteractingpartners |