دورية أكاديمية

Inhibition of KU70 and KU80 by CRISPR interference, not NgAgo interference, increases the efficiency of homologous recombination in pig fetal fibroblasts

التفاصيل البيبلوغرافية
العنوان: Inhibition of KU70 and KU80 by CRISPR interference, not NgAgo interference, increases the efficiency of homologous recombination in pig fetal fibroblasts
المؤلفون: Guo-ling LI, Rong QUAN, Hao-qiang WANG, Xiao-fang RUAN, Jian-xin MO, Cui-li ZHONG, Hua-qiang YANG, Zi-cong LI, Ting GU, De-wu LIU, Zhen-fang WU, Geng-yuan CAI, Xian-wei ZHANG
المصدر: Journal of Integrative Agriculture, Vol 18, Iss 2, Pp 438-448 (2019)
بيانات النشر: Elsevier, 2019.
سنة النشر: 2019
المجموعة: LCC:Agriculture (General)
مصطلحات موضوعية: homologous recombination, non-homologous end-joining, CRISPRi, NgAgoi, KU70, KU80, Agriculture (General), S1-972
الوصف: Non-homologous end-joining (NHEJ) is a predominant pathway for the repair of DNA double-strand breaks (DSB). It inhibits the efficiency of homologous recombination (HR) by competing for DSB targets. To improve the efficiency of HR, multiple CRISPR interference (CRISPRi) and Natronobacterium gregoryi Argonaute (NgAgo) interference (NgAgoi) systems have been designed for the knockdown of NHEJ key molecules, KU70, KU80, polynucleotide kinase/phosphatase (PNKP), DNA ligase IV (LIG4), and NHEJ1. Suppression of KU70 and KU80 by CRISPRi dramatically promoted (P0.05) HR efficiency. Interestingly, although the NgAgoi system significantly suppressed (P0.05) HR efficiency in primary fetal fibroblasts. Our result showed that both NgAgo and catalytically inactive Cas9 (dCas9) could interfere with the expression of target genes, but the downstream factors appear to be more active following CRISPR-mediated interference than that of NgAgo.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2095-3119
Relation: http://www.sciencedirect.com/science/article/pii/S2095311918621501; https://doaj.org/toc/2095-3119
DOI: 10.1016/S2095-3119(18)62150-1
URL الوصول: https://doaj.org/article/2394e1fb94fa4a67917bb9586d404da2
رقم الأكسشن: edsdoj.2394e1fb94fa4a67917bb9586d404da2
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20953119
DOI:10.1016/S2095-3119(18)62150-1