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PUMA1:一种与线虫副蛔虫中的中心体、纺锤体和着丝粒相关联的新型蛋白质。

PUMA1: a novel protein that associates with the centrosomes, spindle and centromeres in the nematode Parascaris.

作者信息

Esteban M R, Giovinazzo G, de la Hera A, Goday C

机构信息

Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

出版信息

J Cell Sci. 1998 Mar;111 ( Pt 6):723-35. doi: 10.1242/jcs.111.6.723.

Abstract

We have identified a 227 kDa spindle- and centromere-associated protein in Parascaris, designated PUMA1 (Parascaris univalens mitotic apparatus), using a monoclonal antibody (mAb403) generated against Parascaris embryonic extracts. PUMA1 distribution was studied by immunofluorescence microscopy in mitotic and meiotic Parascaris cells, where centromere organization differs greatly. In mitosis, PUMA1 associates throughout cell division with the centrosomes and kinetochore-microtubules, and it concentrates at the continuous centromere region of the holocentric chromosomes. PUMA1 also localizes to the spindle mid-zone region during anaphase and at the midbody during telophase. In meiosis, PUMA1 associates with the centrosomes and with the discrete centromeric regions lacking kinetochore structures. The analysis of colchicine-treated embryos indicated that the association of PUMA1 with the centromeric region depends on microtubule integrity. mAb403 also recognizes spindle components in Drosophila. A series of overlapping cDNAs encoding the gene were isolated from a Parascaris embryonic expression library. Analysis of the nucleotide sequence identified an open reading frame capable of encoding a protein of 227 kDa. Analysis of the protein sequence indicated that PUMA1 is predicted to be a coiled-coil protein containing a large central alpha-helical domain flanked by nonhelical terminal domains. The structural features and cellular distribution of PUMA1 suggest that it may play a role in the organization of the spindle apparatus and in its interaction with the centromere in Parascaris.

摘要

我们利用针对蛔虫胚胎提取物产生的单克隆抗体(mAb403),在蛔虫中鉴定出一种227 kDa的纺锤体和着丝粒相关蛋白,命名为PUMA1(单宫蛔虫有丝分裂装置)。通过免疫荧光显微镜研究了PUMA1在有丝分裂和减数分裂的蛔虫细胞中的分布,在这些细胞中着丝粒组织差异很大。在有丝分裂过程中,PUMA1在整个细胞分裂过程中与中心体和动粒微管相关联,并集中在全着丝粒染色体的连续着丝粒区域。在后期,PUMA1也定位于纺锤体中区,在末期定位于中间体。在减数分裂中,PUMA1与中心体以及缺乏动粒结构的离散着丝粒区域相关联。对秋水仙碱处理的胚胎的分析表明,PUMA1与着丝粒区域的关联取决于微管的完整性。mAb403也识别果蝇中的纺锤体成分。从蛔虫胚胎表达文库中分离出一系列编码该基因的重叠cDNA。核苷酸序列分析确定了一个能够编码227 kDa蛋白质的开放阅读框。蛋白质序列分析表明,PUMA1预计是一种卷曲螺旋蛋白,含有一个大的中央α螺旋结构域,两侧是非螺旋末端结构域。PUMA1的结构特征和细胞分布表明,它可能在蛔虫纺锤体装置的组织及其与着丝粒的相互作用中发挥作用。

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