WDR5参与共激活并影响KLF3的基因组靶向性

IF 13.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lu Yang, Manan Shah, Tanit Chavalit, Annalise M Spek, Wooi F Lim, Ling Zhong, Vala Nejad Safari, Mahdi Haddad, Thu H Vu, Joel P Mackay, Mark J Raftery, Marc R Wilkins, Jacqueline M Mathews, Kate G R Quinlan, Merlin Crossley
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引用次数: 0

摘要

kr pel样因子3 (KLF3)是典型的SP/KLF转录因子家族的成员,它通过在启动子和增强子的c末端或附近的三个经典锌指(zf)结合gc -富元件和CACCC盒。KLF3可以抑制和激活转录。它通过其n端结构域招募CtBP共阻遏子来抑制,但其激活机制尚不清楚。在这里,我们发现KLF3与WDR5相互作用,这种相互作用与基因激活有关。我们还证明了这种相互作用对于KLF3的适当基因组靶向是必需的。这有助于解释先前的结果,即KLF3需要c端ZF dna结合域和n端功能域来识别其靶基因。除了促进激活和抑制外,转录共调节因子也可以影响靶基因选择,这一结果只是增加了少数例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WDR5 serves in co-activation and influences genome targeting of KLF3
Krüppel-like factor 3 (KLF3) is a member of the archetypal SP/KLF family of transcription factors that bind GC-rich elements and CACCC boxes in promoters and enhancers via three classical zinc fingers (ZFs) at or near their C-termini. KLF3 can both repress and activate transcription. It represses by recruiting CtBP co-repressors via its N-terminal domain but the mechanism by which it activates was unknown. Here, we show that KLF3 associates with WDR5 and this interaction is associated with gene activation. We also demonstrate that this interaction is required for proper genomic targeting of KLF3. This helps explain previous results indicating that both the C-terminal ZF DNA-binding domain and N-terminal functional domain are required for KLF3 to identify its target genes. This result adds to only a handful of examples that transcriptional co-regulators, in addition to facilitating activation and repression, can also influence target gene selection.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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