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果蝇中心分隔基因在中枢神经系统中线细胞中表达,并编码一种与人类TESK1直系同源的发育调控蛋白激酶。

Drosophila center divider gene is expressed in CNS midline cells and encodes a developmentally regulated protein kinase orthologous to human TESK1.

作者信息

Matthews B B, Crews S T

机构信息

Department of Biochemistry and Biophysics, The University of North Carolina at Chapel Hill 27599-7260, USA.

出版信息

DNA Cell Biol. 1999 Jun;18(6):435-48. doi: 10.1089/104454999315150.

Abstract

The Drosophila center divider gene (cdi) was isolated in an enhancer trap screen undertaken to identify genes involved in embryonic central nervous system (CNS) midline cell development. Three independent lines with P-element insertions at 91F were analyzed that all showed prominent beta-galactosidase expression in the CNS midline precursor cells and other cell types. Null mutations were created by imprecise P-element excision and shown to be larval lethal, although no severe CNS defects were observed in mutant embryos. The DNA surrounding the sites of insertion was cloned and found to contain a transcription unit that was dynamically expressed in a pattern corresponding to the enhancer trap line beta-galactosidase expression. Sequencing of cDNA clones revealed that the cdi gene encodes a 1140-amino acid protein that is an ortholog of the mammalian testis-specific TESK1 protein kinase. This serine/threonine kinase is distinct from other protein kinases because of sequence differences in the residues conferring substrate specificity. The unique sequence is conserved in Cdi, suggesting that Cdi/TESK1 represents a novel class of signaling proteins.

摘要

果蝇中心分隔基因(cdi)是在一项增强子陷阱筛选中分离出来的,该筛选旨在鉴定参与胚胎中枢神经系统(CNS)中线细胞发育的基因。对三个在91F处有P元素插入的独立品系进行了分析,这些品系在CNS中线前体细胞和其他细胞类型中均显示出显著的β-半乳糖苷酶表达。通过不精确的P元素切除产生了无效突变,结果显示这些突变是幼虫致死的,尽管在突变胚胎中未观察到严重的CNS缺陷。对插入位点周围的DNA进行了克隆,发现其包含一个转录单元,该转录单元以与增强子陷阱品系β-半乳糖苷酶表达相对应的模式动态表达。cDNA克隆的测序表明,cdi基因编码一种1140个氨基酸的蛋白质,它是哺乳动物睾丸特异性TESK1蛋白激酶的直系同源物。这种丝氨酸/苏氨酸激酶与其他蛋白激酶不同,因为赋予底物特异性的残基存在序列差异。该独特序列在Cdi中保守,表明Cdi/TESK1代表一类新型的信号蛋白。

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