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拉伸过载引起的幼鸡肥大过程中骨骼肌α-肌动蛋白启动子的调控

Regulation of skeletal alpha-actin promoter in young chickens during hypertrophy caused by stretch overload.

作者信息

Carson J A, Yan Z, Booth F W, Coleman M E, Schwartz R J, Stump C S

机构信息

Department of Physiology and Cell Biology, University of Texas-Houston Health Science Center, USA.

出版信息

Am J Physiol. 1995 Apr;268(4 Pt 1):C918-24. doi: 10.1152/ajpcell.1995.268.4.C918.

Abstract

Anterior latissimus dorsi (ALD) muscles of 3-wk-old male chickens were injected with plasmids containing various lengths of the chicken skeletal alpha-actin promoter (ranging from -2,090 to -77 relative to the transcription start site) driving luciferase. Hypertrophy of the left ALD muscle was induced by attaching a weight (11% of body wt) to the left wing of each chicken, with the unweighted contralateral wing serving the control. Six days of stretch overload significantly increased muscle mass 110%. Luciferase activity from the -2,090 actin-luciferase chimeric gene increased 127% compared with the contralateral control ALD muscle. Luciferase activities driven by the -424, -202, and -99 actin promoters were 179, 134, and 378% higher, respectively, in the stretched ALD muscle than in the contralateral control ALD muscle. Luciferase activity from the -77 deletion construct was not different between stretched and control muscles. These data indicate that the gene region responding to stretch is downstream of -99 and imply, but do not conclusively prove, that the region between -99 and -77, which contains serum response element 1, contributes to the stretch-induced increase in skeletal alpha-actin promoter activity in the ALD muscle.

摘要

给3周龄雄性鸡的背阔肌前部(ALD)注射含有不同长度鸡骨骼肌α-肌动蛋白启动子(相对于转录起始位点从-2,090至-77)驱动荧光素酶的质粒。通过在每只鸡的左翼附着一个重量(体重的11%)诱导左侧ALD肌肉肥大,未加重的对侧翅膀作为对照。6天的拉伸过载使肌肉质量显著增加110%。与对侧对照ALD肌肉相比,-2,090肌动蛋白-荧光素酶嵌合基因的荧光素酶活性增加了127%。在拉伸的ALD肌肉中,由-424、-202和-99肌动蛋白启动子驱动的荧光素酶活性分别比对侧对照ALD肌肉高179%、134%和378%。-77缺失构建体的荧光素酶活性在拉伸和对照肌肉之间没有差异。这些数据表明,响应拉伸的基因区域在-99下游,这意味着但没有确凿证明,包含血清反应元件1的-99和-77之间的区域有助于拉伸诱导的ALD肌肉中骨骼肌α-肌动蛋白启动子活性增加。

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