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果蝇中灯刷状环的进化保守性。

Evolutionary conservation of lampbrush-like loops in drosophilids.

作者信息

Piergentili Roberto

机构信息

Dipartimento di Genetica e Biologia Molecolare, Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185 Rome, Italy.

出版信息

BMC Cell Biol. 2007 Aug 14;8:35. doi: 10.1186/1471-2121-8-35.

Abstract

BACKGROUND

Loopin-1 is an abundant, male germ line specific protein of Drosophila melanogaster. The polyclonal antibody T53-F1 specifically recognizes Loopin-1 and enables its visualization on the Y-chromosome lampbrush-like loop named kl-3 during primary spermatocyte development, as well as on sperm tails. In order to test lampbrush-like loop evolutionary conservation, extensive phase-contrast microscopy and immunostaining with T53-F1 antibody was performed in other drosophilids scattered along their genealogical tree.

RESULTS

In the male germ line of all species tested there are cells showing giant nuclei and intranuclear structures similar to those of Drosophila melanogaster primary spermatocytes. Moreover, the antibody T53-F1 recognizes intranuclear structures in primary spermatocytes of all drosophilids analyzed. Interestingly, the extent and conformation of the staining pattern is species-specific. In addition, the intense staining of sperm tails in all species suggests that the terminal localization of Loopin-1 and its orthologues is conserved. A comparison of these cytological data and the data coming from the literature about sperm length, amount of sperm tail entering the egg during fertilization, shape and extent of both loops and primary spermatocyte nuclei, seems to exclude direct relationships among these parameters.

CONCLUSION

Taken together, the data reported strongly suggest that lampbrush-like loops are a conserved feature of primary spermatocyte nuclei in many, if not all, drosophilids. Moreover, the conserved pattern of the T53-F1 immunostaining indicates that a Loopin-1-like protein is present in all the species analyzed, whose localization on lampbrush-like loops and sperm tails during spermatogenesis is evolutionary conserved.

摘要

背景

Loopin-1是黑腹果蝇中一种丰富的雄性生殖系特异性蛋白质。多克隆抗体T53-F1能特异性识别Loopin-1,并使其在初级精母细胞发育过程中在名为kl-3的Y染色体灯刷样环以及精子尾部上可视化。为了测试灯刷样环的进化保守性,我们在沿着系统发育树分布的其他果蝇中进行了广泛的相差显微镜观察和T53-F1抗体免疫染色。

结果

在所有测试物种的雄性生殖系中,都有细胞显示出巨大的细胞核和与黑腹果蝇初级精母细胞类似的核内结构。此外,抗体T53-F1能识别所有分析的果蝇初级精母细胞中的核内结构。有趣的是,染色模式的范围和构象具有物种特异性。此外,所有物种中精子尾部的强烈染色表明Loopin-1及其直系同源物的末端定位是保守的。将这些细胞学数据与来自文献的关于精子长度、受精过程中进入卵子的精子尾部数量、环和初级精母细胞核的形状及范围的数据进行比较,似乎排除了这些参数之间的直接关系。

结论

综上所述,所报道的数据强烈表明,灯刷样环是许多(如果不是所有)果蝇初级精母细胞核的一个保守特征。此外,T53-F1免疫染色的保守模式表明,在所有分析的物种中都存在一种类似Loopin-1的蛋白质,其在精子发生过程中在灯刷样环和精子尾部的定位是进化保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea3/1978495/6955869e70e0/1471-2121-8-35-1.jpg

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