Department of Biology, University of California at San Diego, La Jolla, California 92093.
Genetics. 1987 Jul;116(3):409-13. doi: 10.1093/genetics/116.3.409.
Males carrying certain X-4 translocations exhibit strongly skewed sperm recovery ratios. The X(P)4(D) half of the translocation disjoins regularly from the Y chromosome and the 4(P)X(D) half disjoins regularly from the normal 4. Yet the smaller member of each bivalent is recovered in excess of its pairing partner, apparently due to differential gametic lethality. Chromosome recovery probabilities are multiplicative; the viability of each genotype is the product of the recovery probability of its component chromosomes. Meiotic drive can also be caused by deficiency for X heterochromatin. In(1)sc(4L)sc(8R) males show the same size dependent chromosome recoveries and multiplicative recovery probabilities found in T(1;4)B(S) males. Meiotic drive in In(1)sc(4L)sc(8R) males has been shown to be due to X-Y pairing failure. Although pairing is regular in the T(X;4) males, the striking phenotypic parallels suggest a common explanation. The experiments described below show that the two phenomena are, in fact, one and the same. X-4 translocations are shown to have the same effect on recovery of independently assorting chromosomes as does In(1)sc(4L)sc(8R). Addition of pairing sites to the 4(P)X(D) half of the translocation eliminates drive. A common explanation-failure of the distal euchromatic portion of the X chromosome to participate in X:Y meiotic pairing-is suggested as the cause for drive. The effect of X chromosome breakpoint on X-4 translocation induced meiotic drive is investigated. It is found that translocations with breakpoints distal to 13C on the salivary map do not cause drive while translocations broken proximal to 13C cause drive. The level of drive is related to the position of the breakpoint-the more proximal the breakpoint the greater the drive.
携带某些 X-4 易位的男性表现出严重偏向的精子回收率。易位的 X(P)4(D) 部分与 Y 染色体正常分离,而 4(P)X(D) 部分与正常 4 正常分离。然而,每个二价体的较小成员的回收率超过其配对伙伴,显然是由于配子致死性的差异。染色体回收率是相乘的;每个基因型的存活率是其组成染色体回收率的乘积。减数分裂驱动也可能由 X 异染色质缺失引起。在 In(1)sc(4L)sc(8R) 男性中,发现与 T(1;4)B(S) 男性相同的大小依赖染色体回收率和乘法回收率概率。In(1)sc(4L)sc(8R) 男性中的减数分裂驱动已被证明是由于 X-Y 配对失败。尽管 T(X;4) 男性中的配对是正常的,但惊人的表型平行表明了一个共同的解释。下面描述的实验表明,这两种现象实际上是一回事。X-4 易位对独立分离染色体的回收具有与 In(1)sc(4L)sc(8R) 相同的影响。在易位的 4(P)X(D) 部分添加配对位点可消除驱动。提出了一个共同的解释,即 X 染色体远端 euchromatic 部分未能参与 X:Y 减数配对,是驱动的原因。研究了 X 染色体断点对 X-4 易位诱导减数分裂驱动的影响。发现唾液图谱上 13C 远端的断点的易位不会引起驱动,而 13C 近端的断点的易位会引起驱动。驱动的水平与断点的位置有关-断点越靠近近端,驱动越大。