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小鼠晶状体发育过程中六种晶状体蛋白转录本的时间调控。

Temporal regulation of six crystallin transcripts during mouse lens development.

作者信息

Goring D R, Breitman M L, Tsui L C

机构信息

Genetics Department, Hospital for Sick Children, Toronto, Canada.

出版信息

Exp Eye Res. 1992 May;54(5):785-95. doi: 10.1016/0014-4835(92)90034-p.

Abstract

Using the polymerase chain reaction (PCR) and RNA blot analysis, we have examined the differential expression patterns of the gamma-crystallins during lens development. Since only four of these genes had been previously characterized, the cDNAs for the remaining two genes, gamma C and gamma F, were isolated and sequenced. The steady-state mRNA profiles were then determined by RNA blot analysis of samples from embryonic stages to 180 days after birth, with gene-specific probes for gamma A, gamma B, gamma C, and gamma D, and a common probe for gamma E and gamma F. Due to the paucity of mismatches between the gamma E and gamma F-crystallin genes, the PCR technique was exploited to determine their relative abundance. The data showed that while all six gamma-crystallin genes were expressed in the embryonic lens, they were differentially regulated during development. At early stages, the levels of gamma B and gamma C mRNAs were found to be relatively low in comparison to those for gamma A, gamma D, gamma E and gamma F. After 30-40 days, however, the levels of gamma A, gamma E, and gamma F mRNAs declined rapidly, and the gamma B, gamma C and gamma D transcripts became the major gamma-crystallin mRNA species. The utility of the PCR technique in studying the relative abundance of steady-state gamma-crystallin mRNAs was also investigated.

摘要

利用聚合酶链反应(PCR)和RNA印迹分析,我们研究了晶状体发育过程中γ-晶状体蛋白的差异表达模式。由于这些基因中此前仅鉴定了四个,因此分离并测序了其余两个基因γC和γF的cDNA。然后,使用针对γA、γB、γC和γD的基因特异性探针以及针对γE和γF的通用探针,通过对从胚胎期到出生后180天的样本进行RNA印迹分析,来确定稳态mRNA图谱。由于γE和γF - 晶状体蛋白基因之间错配较少,因此利用PCR技术来确定它们的相对丰度。数据表明,虽然所有六个γ-晶状体蛋白基因在胚胎晶状体中均有表达,但在发育过程中它们受到不同的调控。在早期阶段,与γA、γD、γE和γF相比,γB和γC mRNA的水平相对较低。然而,在30 - 40天后,γA、γE和γF mRNA的水平迅速下降,γB、γC和γD转录本成为主要的γ-晶状体蛋白mRNA种类。我们还研究了PCR技术在研究稳态γ-晶状体蛋白mRNA相对丰度方面的实用性。

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