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果蝇肌肉节段同源框(msh)基因的正常表达及异位表达效应表明其在胚胎肌肉的分化和模式形成中发挥作用。

Normal expression and the effects of ectopic expression of the Drosophila muscle segment homeobox (msh) gene suggest a role in differentiation and patterning of embryonic muscles.

作者信息

Lord P C, Lin M H, Hales K H, Storti R V

机构信息

Department of Biochemistry M/C 536, University of Illinois, College of Medicine, Chicago 60612, USA.

出版信息

Dev Biol. 1995 Oct;171(2):627-40. doi: 10.1006/dbio.1995.1310.

Abstract

Myogenesis is a several step process that requires genes involved in specifying mesoderm lineage and genes involved in determining muscle identity, differentiation, and patterning. We report here on the isolation, characterization, and expression pattern of a cDNA clone encoded by the previously uncharacterized Drosophila muscle segment homeobox (msh) gene and its possible role in myogenesis. The amino acid sequence of the msh homeobox domain is highly homologous to the homeodomains of the Drosophila S59 and empty spiracles genes and the Hox 7 and Hox 8 family of vertebrate homeobox genes. In addition, the 5' end of msh has 52% sequence identity to the 5' end of the empty spiracles gene and encodes several stretches of amino acids rich in serine, alanine, proline, glutamine, and acidic amino acids, indicating potential domains of regulatory activity. The expression of msh is initially detected at about stage 6 in the dorsal lateral ectoderm of the embryo and later in the developing central (CNS) and peripheral nervous systems. During germ band retraction (stage 12), msh continues to be expressed in cells of the nervous system as well as cells of the somatic mesoderm corresponding mostly to the developing dorsal and lateral somatic body wall muscles. These mesodermal cells, which continue to express msh in daughterless mutant embryos, undergo an increase in cell number in neurogenic mutants. By late stage 14 of embryonic development, msh expression is greatly reduced or absent in most or all mesoderm and muscle but continues in CNS until hatching. Ectopic expression of msh in the mesoderm results in altered expression of the S59 and nau/Dmyd genes leading to a loss of some muscles and defects in the patterning of others, suggesting that the muscle defects are at the level of recruitment and/or patterning of muscle precursor cells. Thus the similarity of Drosophila msh expression to that of the homologous vertebrate Hox 7 and Hox 8 genes together with the effects of ectopic expression of msh in the mesoderm suggest a role for the msh-like family of genes in mesodermal and muscle differentiation and patterning.

摘要

肌生成是一个多步骤过程,需要涉及中胚层谱系特化的基因以及决定肌肉特性、分化和模式形成的基因。我们在此报告一个由先前未被表征的果蝇肌肉节段同源框(msh)基因编码的cDNA克隆的分离、特征及表达模式,以及它在肌生成中可能发挥的作用。msh同源框结构域的氨基酸序列与果蝇S59和空气门基因的同源结构域以及脊椎动物同源框基因的Hox 7和Hox 8家族高度同源。此外,msh的5'端与空气门基因的5'端有52%的序列同一性,并编码几段富含丝氨酸、丙氨酸、脯氨酸、谷氨酰胺和酸性氨基酸的氨基酸序列,表明其具有潜在的调控活性结构域。msh的表达最初在胚胎背外侧外胚层大约第6阶段被检测到,随后在发育中的中枢神经系统(CNS)和外周神经系统中表达。在胚带回缩(第12阶段)期间,msh继续在神经系统细胞以及主要对应于发育中的背侧和外侧体壁肌肉的体壁中胚层细胞中表达。这些中胚层细胞在无女儿突变胚胎中继续表达msh,在神经源性突变体中细胞数量增加。到胚胎发育后期第14阶段,msh在大多数或所有中胚层和肌肉中的表达大大降低或缺失,但在中枢神经系统中持续表达直至孵化。msh在中胚层中的异位表达导致S59和nau/Dmyd基因表达改变,导致一些肌肉缺失和其他肌肉模式形成缺陷,这表明肌肉缺陷发生在肌肉前体细胞的募集和/或模式形成水平。因此,果蝇msh表达与同源脊椎动物Hox 7和Hox 8基因表达的相似性,以及msh在中胚层中的异位表达效应表明,msh样基因家族在中胚层和肌肉分化及模式形成中发挥作用。

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