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秀丽隐杆线虫中 MAP 激酶介导的减数分裂进程的表达谱分析。

Expression profiling of MAP kinase-mediated meiotic progression in Caenorhabditis elegans.

作者信息

Leacock Stefanie W, Reinke Valerie

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America.

出版信息

PLoS Genet. 2006 Nov 10;2(11):e174. doi: 10.1371/journal.pgen.0020174.

DOI:10.1371/journal.pgen.0020174
PMID:17096596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1635537/
Abstract

The LET-60 (Ras)/LIN-45 (Raf)/MPK-1 (MAP kinase) signaling pathway plays a key role in the development of multiple tissues in Caenorhabditis elegans. For the most part, the identities of the downstream genes that act as the ultimate effectors of MPK-1 signaling have remained elusive. A unique allele of mpk-1, ga111, displays a reversible, temperature-sensitive, tissue-specific defect in progression through meiotic prophase I. We performed gene expression profiling on mpk-1(ga111) animals to identify candidate downstream effectors of MPK-1 signaling in the germ line. This analysis delineated a cohort of genes whose expression requires MPK-1 signaling in germ cells in the pachytene stage of meiosis I. RNA in situ hybridization analysis shows that these genes are expressed in the germ line in an MPK-1-dependent manner and have a spatial expression pattern consistent with the location of activated MPK-1. We found that one MPK-1 signaling-responsive gene encoding a C2H2 zinc finger protein plays a role in meiotic chromosome segregation downstream of MPK-1. Additionally, discovery of genes responsive to MPK-1 signaling permitted us to order MPK-1 signaling relative to several events occurring in pachytene, including EFL-1/DPL-1 gene regulation and X chromosome reactivation. This study highlights the utility of applying global gene expression methods to investigate genes downstream of commonly used signaling pathways in vivo.

摘要

LET-60(Ras)/LIN-45(Raf)/MPK-1(丝裂原活化蛋白激酶)信号通路在秀丽隐杆线虫多种组织的发育中起关键作用。在很大程度上,作为MPK-1信号最终效应器的下游基因的身份仍然难以捉摸。mpk-1的一个独特等位基因ga111在减数分裂前期I的进程中表现出可逆的、温度敏感的、组织特异性缺陷。我们对mpk-1(ga111)动物进行了基因表达谱分析,以确定生殖系中MPK-1信号的候选下游效应器。该分析确定了一组基因,其表达在减数分裂I粗线期的生殖细胞中需要MPK-1信号。RNA原位杂交分析表明,这些基因以MPK-1依赖的方式在生殖系中表达,并且具有与活化的MPK-1位置一致的空间表达模式。我们发现一个编码C2H2锌指蛋白的MPK-1信号响应基因在MPK-1下游的减数分裂染色体分离中起作用。此外,对MPK-1信号响应基因的发现使我们能够将MPK-1信号相对于粗线期发生的几个事件进行排序,包括EFL-1/DPL-1基因调控和X染色体重新激活。这项研究强调了应用全局基因表达方法来研究体内常用信号通路下游基因的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c17/1657040/03de5e6b7c81/pgen.0020174.g008.jpg
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