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锌指蛋白-37是KRAB锌指基因家族的成员之一,在发育中和成年中枢神经系统的神经元中表达。

Zfp-37 is a member of the KRAB zinc finger gene family and is expressed in neurons of the developing and adult CNS.

作者信息

Mazarakis N, Michalovich D, Karis A, Grosveld F, Galjart N

机构信息

MGC Department of Cell Biology and Genetics, Erasmus University, Rotterdam, The Netherlands.

出版信息

Genomics. 1996 Apr 15;33(2):247-57. doi: 10.1006/geno.1996.0189.

Abstract

The murine Zfp-37 gene encodes a protein with 12 zinc fingers at its C-terminus (Nelki et al., 1990, Nucleic Acids Res. 18: 3655; Burke and Wolgemuth, 1992, Nucleic Acids Res. 20: 2827-2834). Contrary to the published data, our Northern blot analysis demonstrates not only that the Zfp-37 gene is expressed as 2.3, 2.6, and 4.2 kb mRNAs in testis, but also that there is a 3.7-kb message in the adult mouse brain. Using a partial cDNA as a probe, we have isolated a brain-specific Zfp-37 cDNA clone of 3.3 kb, whose sequence was extended to full length using 5' end RACE. This revealed that the 3.7-kb mRNA is in fact a collection of transcripts with heterogenous 5' ends. Comparison of cDNA and genomic sequences shows that the Zfp-37 gene is spread over a region of approximately 20 kb and consists of six exons, the large 3' end exon containing the complete zinc finger domain, and 3' UTR. Our data show that the Zfp-37 gene utilizes different promoters, alternative splicing, and differential polyadenylation to generate the distinct transcripts of brain and testis. Several protein isoforms are encoded by these mRNAs, some of which contain a truncated form of a conserved domain (Krüppel-associated box) found in other zinc finger genes. In situ hybridization analysis of postnatal brain sections indicates that the Zfp-37 gene is expressed in all neurons of the central nervous system. Together, these results suggest that ZFP-37 is a transcriptional regulator predominantly present in postmitotic cells from two different lineages.

摘要

小鼠Zfp - 37基因在其C末端编码一种含有12个锌指的蛋白质(Nelki等人,1990年,《核酸研究》18: 3655;Burke和Wolgemuth,1992年,《核酸研究》20: 2827 - 2834)。与已发表的数据相反,我们的Northern印迹分析表明,Zfp - 37基因不仅在睾丸中表达为2.3、2.6和4.2 kb的mRNA,而且在成年小鼠大脑中存在一条3.7 kb的信息。使用部分cDNA作为探针,我们分离出了一个3.3 kb的脑特异性Zfp - 37 cDNA克隆,其序列通过5'端RACE扩展至全长。这表明3.7 kb的mRNA实际上是具有异质5'端的转录本集合。cDNA与基因组序列的比较表明,Zfp - 37基因分布在大约20 kb的区域,由六个外显子组成,大的3'端外显子包含完整的锌指结构域和3' UTR。我们的数据表明,Zfp - 37基因利用不同的启动子、可变剪接和差异多聚腺苷酸化来产生大脑和睾丸的不同转录本。这些mRNA编码了几种蛋白质异构体,其中一些包含在其他锌指基因中发现的保守结构域(Krüppel相关盒)的截短形式。对出生后大脑切片的原位杂交分析表明,Zfp - 37基因在中枢神经系统的所有神经元中表达。总之,这些结果表明ZFP - 37是一种主要存在于来自两个不同谱系的有丝分裂后细胞中的转录调节因子。

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