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高等植物的核周微管组织中心和联会复合体共享一种共同抗原:其假定的转移及在减数分裂染色体排序中的作用。

The perinuclear microtubule-organizing center and the synaptonemal complex of higher plants share a common antigen: its putative transfer and role in meiotic chromosomal ordering.

作者信息

Schmit A C, Endlé M C, Lambert A M

机构信息

Institut de Biologie Moléculaire des Plantes du C.N.R.S., UPR 406, Université Louis Pasteur, 12 rue du Général Zimmer, F-67084 Strasbourg Cedex, France.

出版信息

Chromosoma. 1996 Mar;104(6):405-13. doi: 10.1007/BF00352264.

Abstract

Recognition of homologous chromosomes during meiotic prophase is associated in most cases with the formation of the synaptonemal complex along the length of the chromosome. Telomeres, located at the nuclear periphery, are preferential initiation sites for the assembly of the synaptonemal complex. In most eukaryotic cells, telomeres cluster in a restricted area, leading to the "bouquet" configuration in leptotene-zygotene, while this typical organization progressively disappears in late zygotene-pachytene. We wondered whether such striking changes in the intranuclear ordering and pairing of meiotic chromosomes during the progression of prophase I could be correlated with activity of the centrosome and/or microtubule-organizing center (MTOC). Plant cells may be used as a model of special interest for this study as the whole nuclear surface acts as an MTOC, unlike other cell types where MTOCs are restricted to centrosomes or spindle pole bodies. Using a monoclonal antibody (mAb 6C6) raised against isolated calf centrosomes we found that the 6C6 antigen is present over the entire surface of the plant meiotic nucleus, in early prophase I, before chromosomal pairing. At zygotene, short fragments of chromosomes become stained near the nuclear envelope and within the nucleus. At pachytene, after complete synapsis, the labeling specifically concentrates within the synaptonemal complexes, although the nuclear surface is no longer reactive. Ultrastructural localization using immunogold labeling indicates that the 6C6 antigen is colocalized with the synaptonemal complex structures. Later in metaphase I, the antigen is found at the kinetochores. Our data favor the idea that the 6C6 antigen may function as a particular "chromosomal passenger-like" protein. These observations shed new light on the molecular organization of the plant synaptonemal complex and on the redistribution of cytoskeleton-related antigens during initiation of meiosis. They suggest that antigens of MTOCs are relocated to chromosomes during the synapsis process starting at telomeres and contribute to the spatial arrangement of meiotic chromosomes. Such cytoskeleton-related antigens may acquire different functions depending on their localization, which is cell-cycle regulated.

摘要

在减数分裂前期,同源染色体的识别在大多数情况下与沿染色体长度形成联会复合体相关。位于核周边的端粒是联会复合体组装的优先起始位点。在大多数真核细胞中,端粒聚集在一个受限区域,导致细线期-偶线期出现“花束”构型,而这种典型的组织形式在偶线期后期-粗线期逐渐消失。我们想知道在前期I进程中减数分裂染色体的核内排序和配对的这种显著变化是否与中心体和/或微管组织中心(MTOC)的活性相关。植物细胞可作为本研究特别感兴趣的模型,因为与其他细胞类型不同,植物细胞的整个核表面都充当MTOC,而在其他细胞类型中,MTOC局限于中心体或纺锤极体。使用针对分离的小牛中心体制备的单克隆抗体(mAb 6C6),我们发现6C6抗原在前期I早期、染色体配对之前就存在于植物减数分裂核的整个表面。在偶线期,染色体的短片段在核膜附近和核内被染色。在粗线期,完全联会之后,标记物特异性地集中在联会复合体内,尽管核表面不再有反应性。使用免疫金标记的超微结构定位表明6C6抗原与联会复合体结构共定位。在中期I后期,抗原出现在动粒上。我们的数据支持6C6抗原可能作为一种特殊的“类染色体乘客”蛋白发挥作用的观点。这些观察结果为植物联会复合体的分子组织以及减数分裂起始期间细胞骨架相关抗原的重新分布提供了新的线索。它们表明MTOC的抗原在从端粒开始的联会过程中重新定位到染色体上,并有助于减数分裂染色体的空间排列。这种与细胞骨架相关的抗原可能根据其定位获得不同的功能,其定位受细胞周期调控。

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