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首页> 外文期刊>Development >Nucleolar activity and CENP-C regulate CENP-A and CAL1 availability for centromere assembly in meiosis
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Nucleolar activity and CENP-C regulate CENP-A and CAL1 availability for centromere assembly in meiosis

机译:核仁活性和CENP-C调节减数分裂中着丝粒组装的CENP-A和CAL1的可用性

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摘要

The centromere-specific histone CENP-A is the key epigenetic determinant of centromere identity. Whereas most histones are removed from mature sperm, CENP-A is retained to mark paternal centromeres. In Drosophila males we show that the centromere assembly factors CAL1 and CENP-C are required for meiotic chromosome segregation, CENP-A assembly and maintenance on sperm, as well as fertility. In meiosis, CENP-A accumulates with CAL1 in nucleoli. Furthermore, we show that CENP-C normally limits the release of CAL1 and CENP-A from nucleoli for proper centromere assembly in meiotic prophase I. Finally, we show that RNA polymerase I transcription is required for efficient CENP-A assembly in meiosis, as well as centromere tethering to nucleoli.
机译:着丝粒特异性组蛋白CENP-A是着丝粒身份的关键表观遗传决定因素。尽管大多数组蛋白是从成熟精子中去除的,但CENP-A仍保留着标记父本着丝粒的特征。在果蝇雄性中,我们显示着丝粒组装因子CAL1和CENP-C是减数分裂染色体分离,CENP-A组装和精子维持以及生育能力所必需的。在减数分裂中,CENP-A与核仁中的CAL1积累。此外,我们显示CENP-C通常限制减数分裂前期I中适当的着丝粒组装的核仁释放CAL1和CENP-A。最后,我们证明RNA聚合酶I转录是减数分裂中有效CENP-A组装所必需的以及着丝粒拴在核仁上。

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