Suppr超能文献

Csx:一个在发育中的心脏中特异性表达的含小鼠同源异型盒基因。

Csx: a murine homeobox-containing gene specifically expressed in the developing heart.

作者信息

Komuro I, Izumo S

机构信息

Molecular Medicine Divisions, Beth Israel Hospital, Boston, MA 02215.

出版信息

Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8145-9. doi: 10.1073/pnas.90.17.8145.

Abstract

The molecular control of the differentiation process depends in part on lineage-restricted transcription factors that regulate expression of tissue-specific genes. Although significant progress has been made in molecular understanding of skeletal muscle differentiation, no information is available concerning the genes involved in development of the heart, the first organ to form in vertebrate embryos. Many vertebrate homeobox-containing genes have been shown to be expressed in broad regions of the mouse embryo, but no expression of a homeobox gene has been found in the most anterior region of the early embryo, the heart primordium. We report here on the cloning of a murine homeobox cDNA, Csx (cardiac-specific homeobox). The Csx homeodomain sequence is divergent from those of the Hox class genes but is related to that of Drosophila msh-2 (NK-4), which plays a key role in Drosophila heart formation. Csx is conserved in evolution and Csx homologs exist in all vertebrates examined. Transcripts of Csx are detected from the presomite stage (7.5 days postcoitum), when mesoderm differentiates into promyocardium. Csx expression is restricted in the myocardial cells from 8.5 days postcoitum through adult. Csx is not expressed in skeletal or smooth muscle or any other tissues examined. Expression of Csx precedes that of cardiac-specific genes in embryonic stem cells differentiating into beating myocardial cells in vitro. Although physiological function of Csx is yet to be determined, the temporal and spacial pattern of Csx expression raises a possibility that Csx may play a critical role in the differentiation of cardiac cells.

摘要

分化过程的分子调控部分取决于谱系限制转录因子,这些因子调节组织特异性基因的表达。尽管在骨骼肌分化的分子理解方面取得了重大进展,但关于参与脊椎动物胚胎中首个形成的器官——心脏发育的基因,尚无相关信息。许多含脊椎动物同源异型框的基因已被证明在小鼠胚胎的广泛区域表达,但在早期胚胎的最前端区域——心脏原基中,尚未发现同源异型框基因的表达。我们在此报告小鼠同源异型框cDNA(Csx,心脏特异性同源异型框)的克隆。Csx同源异型结构域序列与Hox类基因的序列不同,但与果蝇msh - 2(NK - 4)的序列相关,后者在果蝇心脏形成中起关键作用。Csx在进化过程中保守,在所检测的所有脊椎动物中都存在Csx同源物。从体节形成前阶段(受精后7.5天)就可检测到Csx的转录本,此时中胚层分化为前心肌。从受精后8.5天到成年,Csx的表达局限于心肌细胞。在骨骼肌、平滑肌或所检测的任何其他组织中均未检测到Csx的表达。在体外分化为跳动心肌细胞的胚胎干细胞中,Csx的表达先于心脏特异性基因。尽管Csx的生理功能尚待确定,但Csx表达的时空模式提示Csx可能在心脏细胞的分化中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcd/47305/0d3b58c630d3/pnas01474-0247-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验