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小鼠精子异常水平与主要尿蛋白表型之间的关联。

Linkage between sperm abnormality level and major urinary protein phenotype in mice.

作者信息

Styrna J

机构信息

Department of Genetics and Evolution, Jagiellonian University, Krakow, Poland.

出版信息

Genet Res. 1991 Apr;57(2):135-8. doi: 10.1017/s0016672300029207.

Abstract

Segregation of sperm abnormality level and the pattern of major urinary proteins (MUPs) were investigated in F2 and B1 hybrid males obtained from crosses involving two contrasting inbred strains of mice: CBA/Kw (Mup-1a1a, 3.3% abnormal sperm) and C57BL/Kw (Mup-1b1b, 21.9% abnormal sperm). In the progeny of both crosses mean levels of abnormal spermatozoa were significantly higher for males typed as Mup-1b1b than for heterozygous Mup-1a1b males. Moreover, all F2 hybrid males showing very high percentages of abnormal sperm were Mup-1b1b homozygotes. Similarly, among B1 males with a high level of deformed spermatozoa, a statistically significant majority were Mup-1b1b genotypes. Our results suggest that at least two genes which influence sperm abnormality level are segregating in these crosses. Both appear to be recessive for high sperm abnormality level, and one shows weak linkage to Mup-1 on chromosome 4.

摘要

在通过涉及两种对比鲜明的近交系小鼠(CBA/Kw(Mup-1a1a,3.3%精子异常)和C57BL/Kw(Mup-1b1b,21.9%精子异常))杂交获得的F2和B1杂交雄性小鼠中,研究了精子异常水平与主要尿蛋白(MUPs)模式的分离情况。在两个杂交组合的后代中,被鉴定为Mup-1b1b的雄性小鼠的平均精子异常水平显著高于杂合子Mup-1a1b雄性小鼠。此外,所有显示出极高精子异常百分比的F2杂交雄性小鼠均为Mup-1b1b纯合子。同样,在精子畸形水平较高的B1雄性小鼠中,统计学上显著多数为Mup-1b1b基因型。我们的结果表明,在这些杂交中至少有两个影响精子异常水平的基因正在分离。两者对于高精子异常水平似乎都是隐性的,并且其中一个与4号染色体上的Mup-1表现出弱连锁。

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