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精子发生过程中细胞周期相关蛋白的时序表达:确定减数分裂开始的时间线。

Temporal expression of cell cycle-related proteins during spermatogenesis: establishing a timeline for onset of the meiotic divisions.

作者信息

Inselman A, Eaker S, Handel M A

机构信息

Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN, USA.

出版信息

Cytogenet Genome Res. 2003;103(3-4):277-84. doi: 10.1159/000076813.

Abstract

During spermatogenesis, the complex events of the first meiotic prophase and division phase bring about dramatic changes in nuclear organization. One factor frustrating mechanistic dissection of these events is lack of knowledge about precisely what events occur, in what order they occur, and how they may be interrelated by temporal sequence; in other words, a precise timeline is lacking. This temporal ordering problem can be tackled by following expression and localization in mouse spermatocytes of proteins critical to events of the meiotic cell division process. These include ones that are primarily chromosomal and related to pairing and recombination, as well as kinases and substrates that mediate the cell cycle transition. Distinct and protein-specific patterns occur with respect to expression and localization throughout meiotic prophase and division and dramatic relocalization of proteins occurs as spermatocytes enter the meiotic division phase. This information provides a foundation for a meiotic timeline that can be augmented to provide, eventually, a complete catalog of meiotic events and their temporal sequence. Such a framework can clarify mechanisms of normal meiosis as well as mutant phenotypes and aberrations of the meiotic process that lead to aneuploidy.

摘要

在精子发生过程中,第一次减数分裂前期和分裂期的复杂事件导致核组织发生显著变化。阻碍对这些事件进行机制剖析的一个因素是,我们并不确切了解发生了哪些事件、它们按什么顺序发生,以及它们如何通过时间序列相互关联;换句话说,缺乏精确的时间线。通过追踪对减数分裂细胞分裂过程中的事件至关重要的蛋白质在小鼠精母细胞中的表达和定位,可以解决这个时间排序问题。这些蛋白质包括主要与染色体相关且与配对和重组有关的蛋白质,以及介导细胞周期转变的激酶和底物。在整个减数分裂前期和分裂过程中,蛋白质的表达和定位呈现出独特且具有蛋白质特异性的模式,并且当精母细胞进入减数分裂期时,蛋白质会发生显著的重新定位。这些信息为减数分裂时间线奠定了基础,该时间线可以不断扩充,最终提供减数分裂事件及其时间序列的完整目录。这样一个框架可以阐明正常减数分裂的机制以及导致非整倍体的减数分裂过程的突变表型和畸变。

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