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大鼠鱼精蛋白2基因的表达在转录和翻译水平受到抑制。

Expression of the rat protamine 2 gene is suppressed at the level of transcription and translation.

作者信息

Bunick D, Balhorn R, Stanker L H, Hecht N B

机构信息

Department of Biology, Tufts University, Medford, Massachusetts 02155.

出版信息

Exp Cell Res. 1990 May;188(1):147-52. doi: 10.1016/0014-4827(90)90290-q.

Abstract

We have compared the rat protamine 2 gene sequence (rP2) to that of the mouse protamine 2 (mP2) gene. The sequence encompasses 435 nucleotides of the coding region which includes an intron of 120 nucleotides, 461 nucleotides 5' to the coding sequence and 181 bases 3' to it. In the mouse the protamine 2 gene is abundantly transcribed and translated. The mP2 protein is initially synthesized as a precursor and then proteolytically processed to yield the mature protein. In contrast, in the rat, protamine 2 transcripts are present at 2-5% that found in the mouse and the mature protein has never been detected in spermatozoa. Although there is 92% nucleotide similarity between rat and mouse genes and 91% similarity of the predicted amino acid sequences, in vitro runoff transcription assays performed in either rat or mouse testis-derived transcription systems reveal that the rP2 promoter is only 30% as efficient a promoter as the mP2 promoter. Analyses of total sperm basic nuclear proteins extracted from epididymal sperm using a monoclonal antibody specific for protamine 2 suggest that the rat P2 mRNA is translated in vivo but is not properly processed. These results suggest that the lowered transcription rate and altered processing sites of the rat protamine 2 gene are likely to contribute to the lack of protamine 2 in rat spermatozoa.

摘要

我们已将大鼠鱼精蛋白2基因序列(rP2)与小鼠鱼精蛋白2(mP2)基因序列进行了比较。该序列涵盖编码区的435个核苷酸,其中包括一个120个核苷酸的内含子,编码序列5'端有461个核苷酸,3'端有181个碱基。在小鼠中,鱼精蛋白2基因被大量转录和翻译。mP2蛋白最初以前体形式合成,然后经过蛋白水解加工产生成熟蛋白。相比之下,在大鼠中,鱼精蛋白2转录本的含量仅为小鼠中的2%-5%,且从未在精子中检测到成熟蛋白。尽管大鼠和小鼠基因之间的核苷酸相似性为92%,预测的氨基酸序列相似性为91%,但在大鼠或小鼠睾丸来源的转录系统中进行的体外径流转录分析表明,rP2启动子的效率仅为mP2启动子的30%。使用针对鱼精蛋白2的单克隆抗体对从附睾精子中提取的总精子碱性核蛋白进行分析,结果表明大鼠P2 mRNA在体内被翻译,但加工不当。这些结果表明,大鼠鱼精蛋白2基因转录率降低和加工位点改变可能是大鼠精子中缺乏鱼精蛋白2的原因。

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