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紫海胆胚胎中gatae顺式调控模块的独特发育功能。

Exclusive developmental functions of gatae cis-regulatory modules in the Strongylocentrorus purpuratus embryo.

作者信息

Lee Pei Yun, Nam Jongmin, Davidson Eric H

机构信息

Division of Biology, California Institute of Technology, 1200 E. California Blvd., Mail Code 156-29, Pasadena, CA 9112, USA.

出版信息

Dev Biol. 2007 Jul 15;307(2):434-45. doi: 10.1016/j.ydbio.2007.05.005. Epub 2007 May 10.

DOI:10.1016/j.ydbio.2007.05.005
PMID:17570356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2031225/
Abstract

The gatae gene of Strongylocentrotus purpuratus is orthologous to vertebrate gata-4,5,6 genes. This gene is expressed in the endomesoderm in the blastula and later the gut of the embryo, and is required for normal development. A gatae BAC containing a GFP reporter knocked into exon one of the gene was able to reproduce all aspects of endogenous gatae expression in the embryo. To identify putative gatae cis-regulatory modules we carried out an interspecific sequence conservation analysis with respect to a Lytechinus variegatus gatae BAC, which revealed 25 conserved non-coding sequence patches. These were individually tested in gene transfer experiments, and two modules capable of driving localized reporter expression in the embryo were identified. Module 10 produces early expression in mesoderm and endoderm cells up to the early gastrula stage, while module 24 generates late endodermal expression at gastrula and pluteus stages. Module 10 was then deleted from the gatae BAC by reciprocal recombination, resulting in total loss of reporter expression in the time frame in which it is normally active. Similar deletion of module 24 led to ubiquitous GFP expression in the gastrula and pluteus. These results show that Module 10 is uniquely necessary and sufficient to account for the early phase of gatae expression during endomesoderm specification. In addition, they imply a functional cis-regulatory module exclusion, whereby only a single module can associate with the basal promoter and drive gene expression at any given time.

摘要

紫海胆的gatae基因与脊椎动物的gata - 4、5、6基因是直系同源的。该基因在囊胚期的内胚层中表达,随后在胚胎的肠道中表达,是正常发育所必需的。一个含有敲入该基因外显子1的绿色荧光蛋白(GFP)报告基因的gatae细菌人工染色体(BAC)能够在胚胎中重现内源性gatae表达的所有方面。为了鉴定假定的gatae顺式调控模块,我们对一种多色紫海胆的gatae BAC进行了种间序列保守性分析,结果揭示了25个保守的非编码序列片段。这些片段在基因转移实验中分别进行了测试,鉴定出了两个能够在胚胎中驱动局部报告基因表达的模块。模块10在中胚层和内胚层细胞中产生早期表达,直至早期原肠胚阶段,而模块24在原肠胚和长腕幼虫阶段产生晚期内胚层表达。然后通过反向重组从gatae BAC中删除了模块10,导致报告基因在其正常活跃的时间范围内完全丧失表达。对模块24进行类似的删除导致原肠胚和长腕幼虫中普遍的GFP表达。这些结果表明,模块10对于内胚层中gatae表达的早期阶段是唯一必要且充分的。此外,它们暗示了一种功能性的顺式调控模块排斥,即在任何给定时间只有一个模块能够与基础启动子结合并驱动基因表达。

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