秀丽隐杆线虫nr4a核受体nhr-6发育过程中的结合位点分析。

Nuclear Receptor Research Pub Date : 2017-01-01 Epub Date: 2017-07-23 DOI:10.11131/2017/101288
Brandon Praslicka, Jeremy S Harmson, Joohyun Kim, Vittobai Rashika Rangaraj, Aikseng Ooi, Chris R Gissendanner
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引用次数: 2

摘要

核受体NR4A亚家族的成员组成了一个高度保守、功能多样化的转录因子组,涉及多种细胞过程,如增殖、分化、凋亡、代谢和DNA修复。基因nhr-6编码秀丽隐杆线虫唯一的NR4A核受体同源物,在器官发生和调节精囊器官系统的发育中起关键作用。我们之前的研究表明,nhr-6在L3晚期和L4早期的精囊细胞分裂和L4中期的精囊细胞分化是必需的。在这里,我们利用染色质免疫沉淀和下一代测序(ChIP-seq)来鉴定L3晚期/ L4早期和L4中期发育阶段的NHR-6结合位点。我们的研究结果显示,NHR-6的30,745个富集结合位点,其中约70%位于基因转录起始位点上游3kb内。通过qPCR验证了一组可能在精囊器官发生中起作用的候选靶基因的结合位点。在功能缺失RNAi筛选后,还评估了这些基因的生殖和精膜表型,该筛选显示了在精膜器官发生过程中具有关键功能的几个基因。我们的研究结果揭示了一个复杂的核受体调节网络,其中NHR-6调节精子器官发生过程中的多个细胞过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

BINDING SITE ANALYSIS OF THE <i>CAENORHABDITIS ELEGANS</i> NR4A NUCLEAR RECEPTOR NHR-6 DURING DEVELOPMENT.

BINDING SITE ANALYSIS OF THE <i>CAENORHABDITIS ELEGANS</i> NR4A NUCLEAR RECEPTOR NHR-6 DURING DEVELOPMENT.

BINDING SITE ANALYSIS OF THE <i>CAENORHABDITIS ELEGANS</i> NR4A NUCLEAR RECEPTOR NHR-6 DURING DEVELOPMENT.

BINDING SITE ANALYSIS OF THE CAENORHABDITIS ELEGANS NR4A NUCLEAR RECEPTOR NHR-6 DURING DEVELOPMENT.

Members of the NR4A subfamily of nuclear receptors make up a highly conserved, functionally diverse group of transcription factors implicated in a multitude of cellular processes such as proliferation, differentiation, apoptosis, metabolism and DNA repair. The gene nhr-6, which encodes the sole C. elegans NR4A nuclear receptor homolog, has a critical role in organogenesis and regulates the development of the spermatheca organ system. Our previous work revealed that nhr-6 is required for spermatheca cell divisions in late L3 and early L4 and spermatheca cell differentiation during the mid L4 stage. Here, we utilized chromatin immunoprecipitation followed by next-generation sequencing (ChIP-seq) to identify NHR-6 binding sites during both the late L3/early L4 and mid L4 developmental stages. Our results revealed 30,745 enriched binding sites for NHR-6, ~70% of which were within 3 kb upstream of a gene transcription start site. Binding sites for a cohort of candidate target genes with probable functions in spermatheca organogenesis were validated through qPCR. Reproductive and spermatheca phenotypes were also evaluated for these genes following a loss-of-function RNAi screen which revealed several genes with critical functions during spermatheca organogenesis. Our results uncovered a complex nuclear receptor regulatory network whereby NHR-6 regulates multiple cellular processes during spermatheca organogenesis.

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