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通过功能基因组筛选鉴定减数分裂所必需的基因。

Genes Important for Meiosis Identified Through a Functional Genomics Screen.

机构信息

Wellcome Centre for Cell Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, EH9 3BF, UK.

Institute of Biotechnology, Technische Universität Berlin, 13355 Berlin, Germany.

出版信息

Genetics. 2018 Feb;208(2):589-603. doi: 10.1534/genetics.117.300527. Epub 2017 Dec 19.

DOI:10.1534/genetics.117.300527
PMID:29259000
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5788524/
Abstract

Meiosis is a specialized cell division that generates gametes, such as eggs and sperm. Errors in meiosis result in miscarriages and are the leading cause of birth defects; however, the molecular origins of these defects remain unknown. Studies in model organisms are beginning to identify the genes and pathways important for meiosis, but the parts list is still poorly defined. Here we present a comprehensive catalog of genes important for meiosis in the fission yeast, Our genome-wide functional screen surveyed all nonessential genes for roles in chromosome segregation and spore formation. Novel genes important at distinct stages of the meiotic chromosome segregation and differentiation program were identified. Preliminary characterization implicated three of these genes in centrosome/spindle pole body, centromere, and cohesion function. Our findings represent a near-complete parts list of genes important for meiosis in fission yeast, providing a valuable resource to advance our molecular understanding of meiosis.

摘要

减数分裂是一种特殊的细胞分裂,可产生配子,如卵子和精子。减数分裂过程中的错误会导致流产,也是出生缺陷的主要原因;然而,这些缺陷的分子起源仍不清楚。在模式生物中的研究开始鉴定减数分裂过程中重要的基因和途径,但该部分列表仍定义不佳。在这里,我们呈现了一个在裂殖酵母中减数分裂重要的基因的综合目录。我们的全基因组功能筛选调查了所有非必需基因在染色体分离和孢子形成中的作用。在减数分裂染色体分离和分化程序的不同阶段发现了新的重要基因。初步特征表明,其中三个基因与中心体/纺锤体极体、着丝粒和黏合功能有关。我们的发现代表了裂殖酵母减数分裂中重要基因的近乎完整的部分列表,为我们分子水平理解减数分裂提供了有价值的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/c570df34b6f4/589fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/bec0552dfdc8/589fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/2a3d64c07db5/589fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/d10e62448052/589fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/dfec944213bb/589fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/66a0a813144f/589fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/9b764de9acb0/589fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/c570df34b6f4/589fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/bec0552dfdc8/589fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/2a3d64c07db5/589fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/d10e62448052/589fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/dfec944213bb/589fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/66a0a813144f/589fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/9b764de9acb0/589fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bb2/5788524/c570df34b6f4/589fig7.jpg

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4
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5
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6
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