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对具有雄性不育的三级三体 Ts(512)31H 小鼠精母细胞和卵母细胞的联会复合体分析

Synaptonemal complex analysis in spermatocytes and oocytes of tertiary trisomic Ts(512)31H mice with male sterility.

作者信息

Mahadevaiah S, Mittwoch U

出版信息

Cytogenet Cell Genet. 1986;41(3):169-76. doi: 10.1159/000132222.

Abstract

Whole-mount preparations of silver-stained spermatocytes and oocytes from Ts(512)31H mice were examined in the electron microscope. The 5(12) chromosome was associated with the XY bivalent in the large majority of spermatocytes, whereas in about one-half of the oocytes, the 5(12) was associated with either unpaired chromosomes or heterochromatic parts of chromosomes or showed self-synapsis. There was a tendency for 5(12) chromosomes to be more fully heterochromatic in oocytes than in spermatocytes. A large proportion of oocytes (50%) and a much smaller proportion of spermatocytes exhibited various errors of chromosome pairing, but these proportions were only marginally greater than in control gametocytes from mice with normal karyotypes. It is concluded that the observed errors of pairing bear no simple relation to the almost complete breakdown of spermatogenesis and the marked impairment of oogenesis that occur in tertiary trisomic Ts(5(12))31H mice.

摘要

对 Ts(512)31H 小鼠经银染的精母细胞和卵母细胞整装标本进行了电子显微镜检查。在绝大多数精母细胞中,5(12) 染色体与 XY 二价体相关联,而在约一半的卵母细胞中,5(12) 与未配对的染色体或染色体的异染色质部分相关联,或呈现自我联会。5(12) 染色体在卵母细胞中比在精母细胞中更倾向于完全异染色质化。很大比例的卵母细胞(50%)和小得多比例的精母细胞表现出各种染色体配对错误,但这些比例仅略高于核型正常小鼠的对照配子细胞。得出的结论是,观察到的配对错误与三级三体 Ts(5(12))31H 小鼠中几乎完全的精子发生障碍和明显的卵子发生损伤没有简单的关系。

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