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相关概念视频

Histone Variants at the Centromere02:30

Histone Variants at the Centromere

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Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3...
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Attachment of Sister Chromatids02:57

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As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules.  Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall...
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During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis. 
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At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
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Centrosome Duplication02:25

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The primary microtubule organizing center (MTOC) in animal cells is the centrosome. A centrosome has two cylindrical centrioles at its core. Each centriole consists of nine sets of three microtubules held together by proteins. The centrioles are positioned at right angles to each other and surrounded by a shapeless protein cloud called the pericentriolar matrix, or pericentriolar material (PCM).
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Chromatin Position Affects Gene Expression02:35

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Chromatin is the massive complex of DNA and proteins packaged inside the nucleus. The complexity of chromatin folding and how it is packaged inside the nucleus greatly influences  access to genetic information. Generally, the nucleus' periphery is considered transcriptionally repressive, while the cell's interior is considered a transcriptionally active area. 
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Immunofluorescence Analysis of Endogenous and Exogenous Centromere-kinetochore Proteins
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用于招募效应蛋白的并行途径决定了中间体驱动和抑制

Tomohiro Kumon1, Jun Ma1, R Brian Akins1

  • 1Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA 19104, USA.

Cell
|August 25, 2021
PubMed
概括

自私的中心基因会导致遗传偏差. 中核蛋白进化以抵消这种驱动力,通过抑制基因路径和有利于异性染色体路径,确保稳定的染色体传播.

关键词:
中心分子进化军备竞赛不同染色素动力学介质驱动自私的遗传元素

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科学领域:

  • 遗传学
  • 进化生物学
  • 分子生物学

背景情况:

  • 自私的中间体DNA序列可以在雌性半导体过程中偏向它们的传播,这种现象被称为中间体驱动.
  • 进化论认为,中粒蛋白共同进化以减轻中粒驱动的负面后果.

研究的目的:

  • 在杂交小鼠模型中研究中介质蛋白抑制中介质驱动的分子机制.
  • 确定基因和异性染色体通路在母体和父体中间体之间的功能差异中的作用.

主要方法:

  • 使用具有遗传特异性的母体和父体中间体的杂交小鼠模型.
  • 研究了自私的中心分子DNA利用动态通路和微管破坏稳定的蛋白质.
  • 通过CENP-C等位基因和通过CENP-B删除的异性染色体路径的破坏.
  • 在Murinae基因组上进行分子进化分析.

主要成果:

  • 自私的中心基因组利用动力通道驱动, 招募微管破坏稳定的蛋白质.
  • 一个平行的异色素通路抑制了中间体之间的功能差异.
  • 干扰CENP-C减少了中间体差异,而CENP-B删除则放大了它们.
  • 分子进化揭示了两种途径蛋白质的适应性变化.

结论:

  • 核心蛋白质的进化抑制了自私DNA利用的动态通路.
  • 异性染色素通路的作用是平衡中位素,抵消中位素驱动.
  • 循环进化旨在尽量减少动脉路的利用,同时保持重要的中心分子功能.