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罗伯逊易位Rb(X.2)2Ad对雄性实验小鼠减数分裂I后期不分离的影响。

The influence of the Robertsonian translocation Rb(X.2)2Ad on anaphase I non-disjunction in male laboratory mice.

作者信息

Adler I D, Johannisson R, Winking H

出版信息

Genet Res. 1989 Apr;53(2):77-86. doi: 10.1017/s0016672300027944.

Abstract

A Robertsonian translocation in the mouse between the X chromosome and chromosome 2 is described. The male and female carriers of the Rb(X.2)2Ad were fertile. A homozygous/hemizygous line was maintained. The influence of the X-autosomal Robertsonian translocation on anaphase I non-disjunction in male mice was studied by chromosome counts in cells at metaphase II of meiosis and by assessment of aneuploid progeny. The results conclusively show that the inclusion of Rb2Ad in the male genome induces non-disjunction at the first meoitic division. In second metaphase cells the frequency of sex-chromosomal aneuploidy was 10.8%, and secondary spermatocytes containing two or no sex chromosome were equally frequent. The Rb2Ad males sired 3.9% sex-chromosome aneuploid progeny. The difference in aneuploidy frequencies in the germ cells and among the progeny suggests that the viability of XO and XXY individuals is reduced. The pairing configurations of chromosomes 2, Rb2Ad and Y were studied during meiotic prophase by light and electron microscopy. Trivalent pairing was seen in all well spread nuclei. Complete pairing of the acrocentric autosome 2 with the corresponding segment of the Rb2Ad chromosome was only seen in 3.2% of the cells analysed in the electron microscope. The pairing between the X and Y chromosome in the Rb2Ad males corresponded to that in males with normal karyotype. Reasons for sex-chromosomal non-disjunction despite the normal pairing pattern between the sex chromosomes may be seen in the terminal chiasma location coupled with the asynchronous separation of the sex chromosomes and the autosomes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文描述了小鼠X染色体与2号染色体之间的罗伯逊易位。Rb(X.2)2Ad的雄性和雌性携带者均具有生育能力。维持了一个纯合/半合子品系。通过对减数分裂II中期细胞进行染色体计数以及评估非整倍体后代,研究了X-常染色体罗伯逊易位对雄性小鼠减数分裂I后期不分离的影响。结果确凿地表明,雄性基因组中包含Rb2Ad会在第一次减数分裂时诱导不分离。在第二次中期细胞中,性染色体非整倍体的频率为10.8%,含有两条或没有性染色体的次级精母细胞频率相同。携带Rb2Ad的雄性产生了3.9%的性染色体非整倍体后代。生殖细胞和后代中非整倍体频率的差异表明XO和XXY个体的生存能力降低。通过光学显微镜和电子显微镜研究了减数分裂前期2号染色体、Rb2Ad和Y染色体的配对构型。在所有铺展良好的细胞核中都观察到了三价配对。在电子显微镜分析的细胞中,只有3.2%的细胞中近端着丝粒常染色体2与Rb2Ad染色体的相应片段完全配对。Rb2Ad雄性中X和Y染色体之间的配对与核型正常的雄性中的配对情况一致。尽管性染色体之间的配对模式正常,但性染色体不分离的原因可能在于末端交叉位置以及性染色体和常染色体的不同步分离。(摘要截取自250字)

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