首页> 美国卫生研究院文献>PLoS Clinical Trials >Spag16 an Axonemal Central Apparatus Gene Encodes a Male Germ Cell Nuclear Speckle Protein that Regulates SPAG16 mRNA Expression
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Spag16 an Axonemal Central Apparatus Gene Encodes a Male Germ Cell Nuclear Speckle Protein that Regulates SPAG16 mRNA Expression

机译:Spag16一种轴突中央设备基因编码调控SPAG16 mRNA表达的雄性生殖细胞核斑点蛋白。

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摘要

Spag16 is the murine orthologue of Chlamydomonas reinhardtii PF20, a protein known to be essential to the structure and function of the “9+2” axoneme. In Chlamydomonas, the PF20 gene encodes a single protein present in the central pair of the axoneme. Loss of PF20 prevents central pair assembly/integrity and results in flagellar paralysis. Here we demonstrate that the murine Spag16 gene encodes two proteins: 71 kDa SPAG16L, which is found in all murine cells with motile cilia or flagella, and 35 kDa SPAG16S, representing the C terminus of SPAG16L, which is expressed only in male germ cells, and is predominantly found in specific regions within the nucleus that also contain SC35, a known marker of nuclear speckles enriched in pre-mRNA splicing factors. SPAG16S expression precedes expression of SPAG16L. Mice homozygous for a knockout of SPAG16L alone are infertile, but show no abnormalities in spermatogenesis. Mice chimeric for a mutation deleting the transcripts for both SPAG16L and SPAG16S have a profound defect in spermatogenesis. We show here that transduction of SPAG16S into cultured dispersed mouse male germ cells and BEAS-2B human bronchial epithelial cells increases SPAG16L expression, but has no effect on the expression of several other axoneme components. We also demonstrate that the Spag16L promoter shows increased activity in the presence of SPAG16S. The distinct nuclear localization of SPAG16S and its ability to modulate Spag16L mRNA expression suggest that SPAG16S plays an important role in the gene expression machinery of male germ cells. This is a unique example of a highly conserved axonemal protein gene that encodes two protein products with different functions.
机译:Spag16是莱茵衣藻PF20的鼠直向同源物,该蛋白是已知对“ 9 + 2”轴突蛋白的结构和功能必不可少的蛋白质。在衣藻中,PF20基因编码存在于轴突中心对中的单个蛋白质。 PF20的丢失会阻止中央对的组装/完整性,并导致鞭毛麻痹。在这里,我们证明了鼠Spag16基因编码两种蛋白质:在所有带有活动纤毛或鞭毛的鼠细胞中都发现有71 kDa SPAG16L,而代表SPAG16L C端的35 kDa SPAG16S(仅在雄性生殖细胞中表达),并且主要在细胞核内的特定区域发现,该区域也包含SC35,SC35是已知的富含前mRNA剪接因子的核斑点标记。 SPAG16S的表达在SPAG16L的表达之前。单独敲除SPAG16L的纯合子小鼠是不育的,但在生精过程中未显示异常。嵌合突变的小鼠缺失了SPAG16L和SPAG16S的转录本,在精子发生过程中存在严重缺陷。我们在这里显示SPAG16S到培养的分散的小鼠雄性生殖细胞和BEAS-2B人支气管上皮细胞的转导增加了SPAG16L的表达,但对其他几种轴突成分的表达没有影响。我们还证明了Spag16L启动子在SPAG16S存在下显示出增加的活性。 SPAG16S的独特核定位及其调节Spag16L mRNA表达的能力表明,SPAG16S在雄性生殖细胞的基因表达机制中起着重要作用。这是一个高度保守的轴突蛋白基因的独特例子,该基因编码具有不同功能的两种蛋白产物。

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