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鹌鹑肌分化抗原基因(myoD)受一系列复杂的顺式作用控制序列调控。

Quail myoD is regulated by a complex array of cis-acting control sequences.

作者信息

Pinney D F, de la Brousse F C, Faerman A, Shani M, Maruyama K, Emerson C P

机构信息

Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

出版信息

Dev Biol. 1995 Jul;170(1):21-38. doi: 10.1006/dbio.1995.1192.

DOI:10.1006/dbio.1995.1192
PMID:7601311
Abstract

Quail myoD (QmyoD) is the earliest myoD family member expressed in quail somites and its transcription is initiated in response to early developmental signals. We have investigated the transcriptional regulation of QmyoD to define the cis-acting sequences required for tissue-specific and correct developmental expression. The QmyoD gene locus was isolated and sequenced and its regulatory properties were characterized. We identified three distinct regions of cis-acting regulatory sequences that control the expression of reporter gene constructs following DNA transfection into cell lines and cultured primary quail cells. The first, a complex distal control region (DCR), 11.5 kb upstream of the gene, contains three separable enhancer activities. Two of these DCR enhancer activities are tissue specific and can be autoactivated. In addition, these same two enhancers and the entire DCR direct somite- and muscle-specific expression of a reporter gene in transgenic mice. Sequence analysis of the DCR enhancers reveals clusters of E-boxes, MEF2 binding motifs, and the stretches of sequence identity with the human myoD enhancer. Second, the promoter region has sequences which act positively to direct expression in both muscle and nonmuscle cells as well as sequences that repress expression specifically in nonmuscle cells. The third control region, the PR, is located -3.3 to -5 kb from the transcription start site and directs muscle-specific expression in cultured cells. This analysis demonstrates that QmyoD has multiple control regions and that some features of myoD regulation are conserved between mammals and birds.

摘要

鹌鹑肌细胞生成素(QmyoD)是在鹌鹑体节中最早表达的肌细胞生成素家族成员,其转录是对早期发育信号作出的反应而启动的。我们研究了QmyoD的转录调控,以确定组织特异性和正确发育表达所需的顺式作用序列。分离并测序了QmyoD基因座,并对其调控特性进行了表征。我们鉴定出三个不同的顺式作用调控序列区域,在将DNA转染到细胞系和培养的原代鹌鹑细胞后,这些区域控制报告基因构建体的表达。第一个区域是一个复杂的远端控制区(DCR),位于基因上游11.5 kb处,包含三种可分离的增强子活性。其中两种DCR增强子活性具有组织特异性,并且可以自我激活。此外,这两种相同的增强子和整个DCR在转基因小鼠中指导报告基因的体节和肌肉特异性表达。对DCR增强子的序列分析揭示了E盒、MEF2结合基序的簇,以及与人肌细胞生成素增强子的序列同一性延伸。其次,启动子区域具有在肌肉和非肌肉细胞中都能正向指导表达的序列,以及在非肌肉细胞中特异性抑制表达的序列。第三个控制区域,即PR,位于转录起始位点-3.3至-5 kb处,在培养细胞中指导肌肉特异性表达。该分析表明,QmyoD具有多个控制区域,并且肌细胞生成素调控的一些特征在哺乳动物和鸟类之间是保守的。

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