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多种形式的γ-谷氨酰转肽酶信使核糖核酸在成年大鼠睾丸和附睾中表达。

Multiple forms of gamma-glutamyl transpeptidase messenger ribonucleic acid are expressed in the adult rat testis and epididymis.

作者信息

Palladino M A, Laperche Y, Hinton B T

机构信息

Department of Anatomy and Cell Biology, University of Virginia Health Sciences Center, Charlottesville 22908.

出版信息

Biol Reprod. 1994 Feb;50(2):320-8. doi: 10.1095/biolreprod50.2.320.

Abstract

The expression of gamma-glutamyl transpeptidase (GGT) mRNA in tissues of the adult rat male reproductive tract was examined. Northern blot analysis of total RNA revealed that GGT mRNA expression occurs primarily in the initial segment and caput epididymidis. Multiple GGT mRNAs of varying sizes were detected in the testis and in different regions of the epididymis: testis, 2.4 and 2.8 kb; efferent ducts, 2.2 and 2.5 kb; initial segment, 2.2, 2.4, and 2.5 kb; caput, 2.2, 2.4, and 2.5 kb; corpus, 2.2 and 2.5 kb; cauda, 2.2 and 2.5 kb; ductus deferens, 2.2 and 2.4 kb. Ribonuclease (RNase) H removal of the poly(A) tail from testicular and epididymal GGT mRNA revealed that multiple GGT mRNAs were not generated by differences in the length of the poly(A) tail. Northern blot analysis of poly(A)+ mRNA with four GGT mRNA 5' untranslated region (UTR)-specific cRNA probes showed that the multiple GGT mRNAs expressed in the testis and epididymis were due to differences in the lengths and nucleotide compositions of the 5' UTR. We hypothesize that transcription of multiple GGT mRNAs from different promoters on the single-copy GGT gene is the molecular basis that underlies the region-specific expression of GGT mRNAs along the rat male reproductive tract.

摘要

检测了成年雄性大鼠生殖道组织中γ-谷氨酰转肽酶(GGT)mRNA的表达。对总RNA进行Northern印迹分析显示,GGT mRNA表达主要发生在附睾起始段和头部。在睾丸和附睾的不同区域检测到多种大小不同的GGT mRNA:睾丸,2.4和2.8 kb;输出小管,2.2和2.5 kb;起始段,2.2、2.4和2.5 kb;头部,2.2、2.4和2.5 kb;体部,2.2和2.5 kb;尾部,2.2和2.5 kb;输精管,2.2和2.4 kb。用核糖核酸酶(RNase)H去除睾丸和附睾GGT mRNA的多聚(A)尾表明,多种GGT mRNA不是由多聚(A)尾长度的差异产生的。用四种GGT mRNA 5'非翻译区(UTR)特异性cRNA探针对多聚(A)+ mRNA进行Northern印迹分析表明,睾丸和附睾中表达的多种GGT mRNA是由于5'UTR长度和核苷酸组成的差异。我们推测,从单拷贝GGT基因上不同启动子转录多种GGT mRNA是大鼠雄性生殖道中GGT mRNA区域特异性表达的分子基础。

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