Agul'nik A I, Agul'nik S I, Ruvinskiĭ A O
Genetika. 1990 Oct;26(10):1776-82.
The properties of the t haplotypes, specific mutant states of the proximal region of chromosome 17 in the house mouse keep renewing interest. One such property is increased transmission of the t haplotype from heterozygous t/+ males to their offspring. By means of reciprocal translocation T (16; 17)43H, we have constructed males with tertiary trisomy 17 (+T43/++/RB7+) carrying Robertsonian translocation Rb(16.17)7Bnr. The offspring of these males was viable when sperm of +T43/++ and Rb7+ was used. The segregation patterns in the offspring of t-bearing trisomics were analysed on days 16-18 of embryonic development. It was found that in the case when the t haplotype is on the normal acrocentric (male male ++T43/+t12+/Rb7++), its presence in the gamete +t12+/++T43 does not produce meiotic drive. However, when t6 is on Rb7, meiotic drive was equal to 80%. It is concluded that the presence of a normal homolog and a t-bearing chromosome in sperm does not result in meiotic drive. Possible mechanisms of meiotic drive of the t haplotypes are discussed.
小家鼠17号染色体近端区域的特定突变状态——t单倍型的特性一直引发着人们的兴趣。其中一个特性是t单倍型从杂合子t/+雄性向其后代的传递增加。通过相互易位T(16;17)43H,我们构建了携带罗伯逊易位Rb(16.17)7Bnr的17号染色体三级三体(+T43/++/RB7+)雄性个体。当使用+T43/++和Rb7+的精子时,这些雄性个体的后代是可存活的。在胚胎发育的第16至18天分析了携带t的三体后代的分离模式。结果发现,当t单倍型位于正常近端着丝粒染色体上时(雄性雄性++T43/+t12+/Rb7++),其在配子+t12+/++T43中的存在不会产生减数分裂驱动。然而,当t6位于Rb7上时,减数分裂驱动等于80%。得出的结论是,精子中正常同源染色体和携带t的染色体的存在不会导致减数分裂驱动。文中讨论了t单倍型减数分裂驱动的可能机制。