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性连锁矮小来航鸡生长激素受体基因表达:排除基因缺失的证据

Growth hormone receptor gene expression in sex-linked dwarf Leghorn chickens: evidence against a gene deletion.

作者信息

Hull K L, Fraser R A, Marsh J A, Harvey S

机构信息

Department of Physiology, University of Alberta, Edmonton, Canada.

出版信息

J Endocrinol. 1993 Apr;137(1):91-8. doi: 10.1677/joe.0.1370091.

Abstract

GH receptor (GHR) mRNA has been identified in peripheral (liver and muscle) and central (brain and hypothalamus) tissues of sex-linked dwarf (SLD) Leghorn chickens. Total RNA was extracted from the tissues of immature (1 week, 4 week), pubertal (16 week) and adult (> 24 weeks) SLD and K (the normally growing strain) Leghorn chickens. In both groups and all tissues, an mRNA moiety of 4.4 kb hybridized with cRNA probes derived from the rabbit hepatic GHR sequence. An additional low-abundance transcript of 2.8 kb was also identified in some tissues. An age-related increase in expression was observed in K and SLD hepatic GHR mRNA, suggesting normal regulation of SLD GHR gene transcription. Amplification of cDNA from K and SLD tissues in the presence of oligonucleotide primers coding for the intracellular or extracellular domains of the chicken GHR generated electrophoretically separable fragments of expected size. Restriction enzyme digestion of the products with EcoRI, BstNI, HaeIII, NcoI or BamHI produced smaller moieties of expected sizes in both strains. These results demonstrate that, in contrast to broiler SLDs, a GHR gene deletion is not responsible for the GHR dysfunction in Leghorn SLDs. Although the actual defect in GHR gene expression in SLD Leghorns remains to be identified, this study demonstrates that sex-linked dwarfism, like Laron dwarfism, is due to a heterogeneity of lesions.

摘要

已在性连锁矮小(SLD)来航鸡的外周组织(肝脏和肌肉)和中枢组织(大脑和下丘脑)中鉴定出生长激素受体(GHR)mRNA。从未成熟(1周、4周)、青春期(16周)和成年(>24周)的SLD和K(正常生长品系)来航鸡的组织中提取总RNA。在两组所有组织中,一个4.4 kb的mRNA部分与源自兔肝脏GHR序列的cRNA探针杂交。在一些组织中还鉴定出一个额外的低丰度2.8 kb转录本。在K和SLD肝脏GHR mRNA中观察到与年龄相关的表达增加,表明SLD GHR基因转录受到正常调控。在编码鸡GHR细胞内或细胞外结构域的寡核苷酸引物存在下,对K和SLD组织的cDNA进行扩增,产生了预期大小的可通过电泳分离的片段。用EcoRI、BstNI、HaeIII、NcoI或BamHI对产物进行限制性酶切,在两个品系中均产生了预期大小的较小部分。这些结果表明,与肉鸡SLD不同,GHR基因缺失不是来航鸡SLD中GHR功能障碍的原因。虽然SLD来航鸡GHR基因表达的实际缺陷仍有待确定,但这项研究表明,性连锁矮小症与拉伦侏儒症一样,是由于病变的异质性。

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