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与小鼠生精细胞凋亡相关的MSRG-11基因的分子克隆

Molecular cloning of MSRG-11 gene related to apoptosis of mouse spermatogenic cells.

作者信息

Deng Yun, Nie Dong-Song, Wang Jian, Tan Xiao-Jun, Nie Zhao-Yan, Yang Hong-Mei, Hu Liang-Sha, Lu Guang-Xiu

机构信息

Human Reproductive and Stem Cell Engineering Institute, Central South University, Changsha, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2005 Mar;37(3):159-66.

Abstract

Beginning with a new contig of the expressed sequence tags (Mm.63892) obtained by comparing testis libraries with other tissue and cell line libraries using the digital differential display program, we cloned a new gene which is related to the apoptosis of mouse spermatogenic cells using the Genscan program and polymerase chain reaction (PCR) technology. The sequence data have been submitted to the GenBank database under accession number AY747687. The full cDNA length is 1074 bp, and the gene with 7 exons and 6 introns is located in mouse chromosome 1 H5. The protein is recognized as a new member of calmodulin (CaM) binding protein family because the sequence contains three short calmodulin-binding motifs containing conserved Ile and Gln residues (IQ motif) and is considered to play a critical role in interactions of IQ motif-containing proteins with CaM proteins. The putative protein encoded by this gene has 192 amino acid residues with a theoretical molecular mass of 23.7 kDa and a calculated isoelectric point of 9.71. The sequence shares no significant homology with any known protein in databases. RT-PCR and Northern blot analyses revealed that 1.3 kb MSRG-11 transcript was strongly expressed in adult mouse testis but weakly expressed in the spleen and thymus. The MSRG-11 gene was expressed at various levels, faintly at two weeks postpartum and strongly from three weeks postpartum in adult testes. The green fluorescence produced by pEGFP-C2/MSRG-11 was detected in the cytoplasm of COS7 cells 24 h post-transfection. The pcDNA3.1(?-)/MSRG-11 plasmid was constructed and introduced into COS7 cells using Lipofectamine 2000 transfection reagent (Invitrogen, Carlsbad, USA). MSRG-11 can accelerate COS7 cell apoptosis, which suggests that this gene may play an important role in the development of mouse testes and is a candidate gene of testis-specific apoptosis. Based on these observations, it was considered that we cloned a new gene which probably accelerates spermatogenetic cell apoptosis in mouse.

摘要

从通过使用数字差异显示程序将睾丸文库与其他组织和细胞系文库进行比较而获得的表达序列标签(Mm.63892)的新重叠群开始,我们使用基因扫描程序和聚合酶链反应(PCR)技术克隆了一个与小鼠生精细胞凋亡相关的新基因。序列数据已提交至GenBank数据库,登录号为AY747687。完整的cDNA长度为1074 bp,该基因有7个外显子和6个内含子,位于小鼠1号染色体H5区域。该蛋白质被认为是钙调蛋白(CaM)结合蛋白家族的新成员,因为其序列包含三个含有保守异亮氨酸和谷氨酰胺残基的短钙调蛋白结合基序(IQ基序),并被认为在含IQ基序的蛋白质与CaM蛋白的相互作用中起关键作用。该基因编码的推定蛋白质有192个氨基酸残基,理论分子量为23.7 kDa,计算得到的等电点为9.71。该序列与数据库中任何已知蛋白质均无明显同源性。逆转录聚合酶链反应(RT-PCR)和Northern印迹分析表明,1.3 kb的MSRG-11转录本在成年小鼠睾丸中强烈表达,但在脾脏和胸腺中弱表达。MSRG-11基因在成年睾丸中的表达水平各不相同,产后两周时微弱表达,产后三周起强烈表达。转染24小时后,在COS7细胞的细胞质中检测到pEGFP-C2/MSRG-11产生的绿色荧光。构建了pcDNA3.1(+)/MSRG-11质粒,并使用Lipofectamine 2000转染试剂(美国加利福尼亚州卡尔斯巴德的英杰公司)将其导入COS7细胞。MSRG-11可加速COS7细胞凋亡,这表明该基因可能在小鼠睾丸发育中起重要作用,是睾丸特异性凋亡的候选基因。基于这些观察结果,我们认为克隆了一个可能加速小鼠生精细胞凋亡的新基因。

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