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A MODIFIED MODEL OF SEGREGATION DISTORTION IN DROSOPHILA MELANOGASTER
Author(s) -
Yuichiro Hiraizumi,
Diana W. Martin,
Irene Eckstrand
Publication year - 1980
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/95.3.693
Subject(s) - repressor , locus (genetics) , biology , drosophila melanogaster , allele , genetics , inducer , microbiology and biotechnology , gene , transcription factor
Elements of the Segregation Distorter (SD) system of Drosophila melanogaster, Sd and Rsp, were analyzed and the following points were established: (1) The model of multiple alleles at the Rsp  s locus proposed by MARTIN and HIRAIZUMI (1979) is supported by our observations. (2) A modifier of SD, tentatively symbolized M(SD), was found close to cn (2R-57.5). (3) Sd heterozygous males were found to show, under certain genotypic condition, almost complete sterility.——Based upon these observations, the following modified model of segregation distortion is proposed: (1) The M(SD) locus produces a multimeric repressor protein that binds to the Rsp locus as a necessary condition for normal spermiogenesis. M(SD) homozygotes produce a repressor M(SD)/M(SD); whereas, a homozygote for its normal allele M+(SD) produces a M+(SD)/M+(SD) repressor. M(SD)/M+(SD) heterzygotes produce a M(SD)/M+(SD) repressor. (2) The Sd locus produces a certain product that, like an inducer in the lactose system of E. coli, tends to bind with the repressor complexed with the Rsp locus. This binding disrupts the repressor-Rsp complex, causing Rsp locus to be turned on. The product of Rsp transcription, in turn, results in sperm dysfunction. (3) Rsp  i, an allele of Rsp, has a strong complexing affinity with the repressor such that the Rsp  i-repressor complex is "resistant" to the inducing activity of Sd product. Rsp  s, on the other hand, has a weaker complexing affinity than that of Rsp  i, and the degree of affinity varies among different Rsp  s alleles.——A possible extension of the above model is discussed.

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