دورية أكاديمية

ATM and ATR checkpoint kinase pathways: A concise review

التفاصيل البيبلوغرافية
العنوان: ATM and ATR checkpoint kinase pathways: A concise review
المؤلفون: Varsha Wagh, Pranav Joshi, Heena Jariyal, Neelam Chauhan
المصدر: Advances in Human Biology, Vol 10, Iss 2, Pp 51-59 (2020)
بيانات النشر: Wolters Kluwer Medknow Publications, 2020.
سنة النشر: 2020
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: 9-1-1 complex, ataxia-telangiectasia-mutated and rad3-related, ataxia-telangiectasia-mutated, checkpoint kinase 1, checkpoint kinase 2, dna damage repair pathway, mre11– rad50–nbs1 complex, Biology (General), QH301-705.5
الوصف: The ataxia-telangiectasia-mutated (ATM) and ataxia-telangiectasia-mutated and Rad3-related (ATR) DNA damage repair pathways serve as the surveillance system which keeps a check on different types of DNA damages and lesions, which includes DNA single-strand breaks, DNA double-strand breaks and other aberrant structures such as arrested replication forks during replication. The ATM and ATR kinases belong to PIKK class of kinases which activate a large number of downstream mediator and effector molecules. The main classes of effector kinases activated by ATM and ATR are checkpoint kinase 2 and checkpoint kinase 1, respectively. ATR works primarily with the RAD9-RAD1-HUS1 (9-1-1) complex, whereas ATM works with the MRE11– RAD50–NBS1 complex. Together ATM and ATR kinase protects the cells' genomic integrity and prevents random mutations to be carried into their progeny.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2321-8568
2348-4691
41858360
العلاقة: http://www.aihbonline.com/article.asp?issn=2321-8568;year=2020;volume=10;issue=2;spage=51;epage=59;aulast=WaghTest; https://doaj.org/toc/2321-8568Test; https://doaj.org/toc/2348-4691Test
DOI: 10.4103/AIHB.AIHB_78_19
الوصول الحر: https://doaj.org/article/a779fa9ec1bd418583608edc5590235eTest
رقم الانضمام: edsdoj.779fa9ec1bd418583608edc5590235e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23218568
23484691
41858360
DOI:10.4103/AIHB.AIHB_78_19