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具有成体合胞体生殖系膜结构缺陷的温度敏感型秀丽隐杆线虫突变体的高通量克隆

High-Throughput Cloning of Temperature-Sensitive Caenorhabditis elegans Mutants with Adult Syncytial Germline Membrane Architecture Defects.

作者信息

Lowry Josh, Yochem John, Chuang Chien-Hui, Sugioka Kenji, Connolly Amy A, Bowerman Bruce

机构信息

Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403.

Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403

出版信息

G3 (Bethesda). 2015 Aug 26;5(11):2241-55. doi: 10.1534/g3.115.021451.

Abstract

The adult Caenorhabditis elegans hermaphrodite gonad consists of two mirror-symmetric U-shaped arms, with germline nuclei located peripherally in the distal regions of each arm. The nuclei are housed within membrane cubicles that are open to the center, forming a syncytium with a shared cytoplasmic core called the rachis. As the distal germline nuclei progress through meiotic prophase, they move proximally and eventually cellularize as their compartments grow in size. The development and maintenance of this complex and dynamic germline membrane architecture are relatively unexplored, and we have used a forward genetic screen to identify 20 temperature-sensitive mutations in 19 essential genes that cause defects in the germline membrane architecture. Using a combined genome-wide SNP mapping and whole genome sequencing strategy, we have identified the causal mutations in 10 of these mutants. Four of the genes we have identified are conserved, with orthologs known to be involved in membrane biology, and are required for proper development or maintenance of the adult germline membrane architecture. This work provides a starting point for further investigation of the mechanisms that control the dynamics of syncytial membrane architecture during adult oogenesis.

摘要

成年秀丽隐杆线虫雌雄同体的性腺由两个镜像对称的U形臂组成,生殖细胞核位于每个臂远端的周边。这些细胞核位于向中心开放的膜小室内,形成一个具有称为轴的共享细胞质核心的合胞体。随着远端生殖细胞核经历减数分裂前期,它们向近端移动,并最终随着其隔室大小的增加而细胞化。这种复杂且动态的生殖系膜结构的发育和维持相对未被探索,我们通过正向遗传筛选在19个必需基因中鉴定出20个温度敏感突变,这些突变导致生殖系膜结构缺陷。使用全基因组SNP定位和全基因组测序相结合的策略,我们已经鉴定出其中10个突变体的致病突变。我们鉴定出的四个基因是保守的,其直系同源基因已知参与膜生物学,并且是成年生殖系膜结构正常发育或维持所必需的。这项工作为进一步研究成年卵子发生过程中控制合胞体膜结构动态的机制提供了一个起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e47/4632044/8dbcebf0c948/2241f1.jpg

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