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H-2复合体内减数分裂重组的性偏好。

Sexual preference of meiotic recombination within the H-2 complex.

作者信息

Shiroishi T, Sagai T, Moriwaki K

出版信息

Immunogenetics. 1987;25(4):258-62. doi: 10.1007/BF00404696.

Abstract

The recombination frequency between the H-2K and H-2D marker loci in male mice was measured using heterozygotes that carry the H-2wm7 haplotype derived from the Japanese wild mouse and common H-2 haplotypes derived from inbred mice. Previous mating experiments in which backcross progeny of heterozygous females were screened demonstrated that the H-2wm7 displays marked enhancement of recombination within the H-2 complex. In contrast to recombination in female mice, no enhancement of recombination was observed during male meiosis in the present study. Thus, it appeared that enhancement of recombination is specific to female mice. A genealogical study of recombination indicated that the postmeiotic stage is not involved in the generation of sexual preference of enhancement of recombination, suggesting that the preference is meiotic-drive and that a female-specific mechanism is involved in meiotic recombination mediated by the H-2wm7 haplotype.

摘要

利用携带源自日本野生小鼠的H-2wm7单倍型和源自近交系小鼠的常见H-2单倍型的杂合子,测量雄性小鼠中H-2K和H-2D标记基因座之间的重组频率。先前对杂合雌性回交后代进行筛选的交配实验表明,H-2wm7在H-2复合体内显示出明显的重组增强。与雌性小鼠的重组情况相反,在本研究中,雄性减数分裂过程中未观察到重组增强。因此,似乎重组增强是雌性小鼠特有的。一项关于重组的谱系研究表明,减数分裂后阶段不参与重组增强的性别偏好的产生,这表明这种偏好是减数分裂驱动的,并且一种雌性特异性机制参与了由H-2wm7单倍型介导的减数分裂重组。

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