首页> 外文期刊>Development >The testis-specific proteasome subunit Prosalpha6T of D. melanogaster is required for individualization and nuclear maturation during spermatogenesis.
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The testis-specific proteasome subunit Prosalpha6T of D. melanogaster is required for individualization and nuclear maturation during spermatogenesis.

机译:D. melanogaster的睾丸特异性蛋白酶体亚基Prosalpha6T是精子发生过程中个体化和核成熟所必需的。

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Most regulated proteolysis in eukaryotes is carried out by the 26S proteasome. This large, multisubunit complex comprises a catalytic core particle (20S proteasome) and a regulatory particle (19S regulator) capping each end. In Drosophila, about a third of the 32 proteasome subunits are found to have testis-specific isoforms, encoded by paralogous genes. Here, we characterize in detail the spermatogenic expression of the core particle subunit Prosalpha6 (Pros35) and its testis-specific isoform Prosalpha6T. Using GFP-tagged transgenes, it is shown that whereas the Prosalpha6 subunit is expressed in early stages of spermatogenesis, gradually fading away following meiosis, the testis-specific Prosalpha6T becomes prominent in spermatid nuclei and cytoplasm after meiosis, and persists in mature sperm. In addition, these subunits are found in numerous ;speckles' near individualization complexes, similar to the previously described expression pattern of the caspase Dronc (Nedd2-like caspase), suggesting a link to the apoptosis pathway. We also studied the phenotypes of a loss-of-function mutant of Prosalpha6T generated by targeted homologous recombination. Homozygous males are sterile and show spermatogenic defects in sperm individualization and nuclear maturation, consistent with the expression pattern of Prosalpha6T. The results demonstrate a functional role of testis-specific proteasomes during Drosophila spermatogenesis.
机译:真核生物中最受调节的蛋白水解是由26S蛋白酶体进行的。这种大的多亚基复合物包含一个催化核心颗粒(20S蛋白酶体)和一个覆盖每个末端的调节颗粒(19S调节剂)。在果蝇中,发现32个蛋白酶体亚基中约有1/3具有睾丸特异性同种型,由同源基因编码。在这里,我们详细表征核心粒子亚基Prosalpha6(Pros35)及其睾丸特异性同工型Prosalpha6T的生精表达。使用GFP标记的转基因表明,虽然Prosalpha6亚基在精子发生的早期阶段表达,在减数分裂后逐渐消失,而睾丸特异性Prosalpha6T在减数分裂后在精子细胞核和细胞质中变得突出,并在成熟的精子中持续存在。此外,这些亚基存在于大量斑点附近的个体化复合物中,类似于先前描述的胱天蛋白酶Dronc(Nedd2样胱天蛋白酶)的表达模式,表明与凋亡途径有关。我们还研究了靶向同源重组产生的Prosalpha6T功能丧失突变体的表型。纯合子雄性不育,在精子个体化和核成熟中表现出生精缺陷,与Prosalpha6T的表达模式一致。结果表明果蝇精子发生过程中睾丸特异性蛋白酶体的功能作用。

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