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利用一种脊椎动物心脏特化基因挽救秀丽隐杆线虫的咽部发育。

Rescue of Caenorhabditis elegans pharyngeal development by a vertebrate heart specification gene.

作者信息

Haun C, Alexander J, Stainier D Y, Okkema P G

机构信息

Department of Biological Sciences, University of Illinois at Chicago, Chicago, IL 60607, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Apr 28;95(9):5072-5. doi: 10.1073/pnas.95.9.5072.

Abstract

Development of pharyngeal muscle in nematodes and cardiac muscle in vertebrates and insects involves the related homeobox genes ceh-22, nkx2.5, and tinman, respectively. To determine whether the nematode and vertebrate genes perform similar functions, we examined activity of the zebrafish nkx2.5 gene in transgenic Caenorhabditis elegans. Here, we report that ectopic expression of nkx2.5 in C. elegans body wall muscle can directly activate expression of both the endogenous myo-2 gene, a ceh-22 target normally expressed only in pharyngeal muscle, and a synthetic reporter construct controlled by a multimerized CEH-22 binding site. nkx2.5 also efficiently rescues a ceh-22 mutant when expressed in pharyngeal muscle. Together, these results indicate that nkx2.5 and ceh-22 provide a single conserved molecular function. Further, they suggest that an evolutionarily conserved mechanism underlies heart development in vertebrates and insects and pharyngeal development in nematodes.

摘要

线虫咽肌以及脊椎动物和昆虫心肌的发育分别涉及相关的同源异型框基因ceh - 22、nkx2.5和tinman。为了确定线虫和脊椎动物的基因是否具有相似功能,我们检测了斑马鱼nkx2.5基因在转基因秀丽隐杆线虫中的活性。在此,我们报告nkx2.5在秀丽隐杆线虫体壁肌肉中的异位表达可直接激活内源性myo - 2基因(一种通常仅在咽肌中表达的ceh - 22靶基因)以及由多聚化CEH - 22结合位点控制的合成报告基因构建体的表达。当在咽肌中表达时,nkx2.5也能有效挽救ceh - 22突变体。这些结果共同表明,nkx2.5和ceh - 22具有单一保守的分子功能。此外,它们表明脊椎动物和昆虫心脏发育以及线虫咽发育背后存在一种进化上保守的机制。

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