Aging effect on the phenomenon of segregation distortion in Drosophila melanogaster.
Aging effect on the phenomenon of segregation distortion in Drosophila melanogaster.
复制标题
衰老对果蝇分离扭曲现象的影响。
作者:
Y. Hiraizumi;S. Watanabe
EGREGATION Distorter (SD) is an element located in the centromeric region sof chromosome 2 of Drosophila mlanogaster. When a male carries SD in heterozygous condition, it transmits SD to its progeny in a great excess over the theoretical frequency of 50%. The SD system consists of three major elements: the SD locus itself which is the element causing segregation distortion; Activator of SD, Ac(SD), which is located to the right and close to the SD locus and is necessary, in coupling, for SD to function; and Stabilizer of SD, St(SD), which is located at the tip of the right arm of chromosome 2 and has a function, either in coupling or in repulsion phase, to stabilize, or enhance the SD action. For further information on SD, the reader may refer to the following papers: SANDLER, HIRAIZUMI and SANDLER (1959), SANDLER and HIRAIZUMI (1960a, b) , SANDLER and HIRAIZUMI (1961 ) , PEACOCK and ERICKSON (1 965), HIRAIZUMI and NAKAZIMA (1967), HARTL, HIRAIZUMI and CROW (1967). In 1961, SANDLER and HIRAIZUMI reported that when a SD heterozygous male was aged the intensity of segregation distortion was remarkably reduced: if k is the proportion of SD progeny flies recovered in the F, generation of the mating, SD+/SD+ o 0 X SD/SD+ 8 8 , k decreased when the SD males got old. However they were unable to show which of the three elements, SD, Ac(SD), or St(SD), was responsible for the aging effect nor were they able to show whether the decrease in k was due to an increase in the number of SD+, or due to a decrease in the number of SD progeny. The purpose of the present study is (1 ) to present data for the aging effect on k values of males carrying various elements of the SD system and ( 2 ) to show that the decrease in k with increasing age of the male is in fact due to an increase in the number of SD+ progeny, but that the number of SD progeny is independent of the aging effect.