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从早期同源物识别到联会复合体形成。

From early homologue recognition to synaptonemal complex formation.

作者信息

Zickler Denise

机构信息

Université Paris-Sud, Institut de Génétique et Microbiologie, 91405, Orsay, France.

出版信息

Chromosoma. 2006 Jun;115(3):158-74. doi: 10.1007/s00412-006-0048-6. Epub 2006 Mar 29.

Abstract

This review focuses on various aspects of chromosome homology searching and their relationship to meiotic and vegetative pairing and to the silencing of unpaired copies of genes. Chromosome recognition and pairing is a prominent characteristic of meiosis; however, for some organisms, this association (complete or partial) is also a normal part of nuclear organization. The multiple mechanisms suggested to contribute to homologous pairing are analyzed. Recognition of DNA/DNA homology also plays an important role in detecting DNA segments that are present in inappropriate number of copies before and during meiosis. In this context, the mechanisms of methylation induced premeiotically, repeat-induced point mutation, meiotic silencing by unpaired DNA, and meiotic sex chromosome inactivation will be discussed. Homologue juxtaposition during meiotic prophase can be divided into three mechanistically distinct steps, namely, recognition, presynaptic alignment, and synapsis by the synaptonemal complex (SC). In most organisms, these three steps are distinguished by their dependence on DNA double-strand breaks (DSBs). The coupling of SC initiation to (and downstream effects of) DSB formation and the exceptions to this dependency are discussed. Finally, this review addresses the specific factors that appear to promote chromosome movement at various stages of meiotic prophase, most particularly at the bouquet stage, and on their significance for homologue pairing and/or achieving a final pachytene configuration.

摘要

本综述聚焦于染色体同源性搜索的各个方面,以及它们与减数分裂和营养体配对以及未配对基因拷贝沉默的关系。染色体识别和配对是减数分裂的一个显著特征;然而,对于某些生物体来说,这种关联(完全或部分)也是核组织的正常组成部分。分析了被认为有助于同源配对的多种机制。DNA/DNA同源性的识别在检测减数分裂前和减数分裂期间拷贝数不合适的DNA片段中也起着重要作用。在这种背景下,将讨论减数分裂前诱导的甲基化机制、重复诱导的点突变、未配对DNA导致的减数分裂沉默以及减数分裂性染色体失活。减数分裂前期同源染色体的并列可分为三个机制上不同的步骤,即识别、突触前排列和通过联会复合体(SC)进行的联会。在大多数生物体中,这三个步骤的区别在于它们对DNA双链断裂(DSB)的依赖性。讨论了SC起始与DSB形成的耦合(以及其下游效应)以及这种依赖性的例外情况。最后,本综述探讨了在减数分裂前期各个阶段,尤其是在花束期,似乎促进染色体运动的特定因素,以及它们对同源配对和/或实现最终粗线期构型的意义。

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