Abstract:Mitosis is the process whereby a cell separates its paired chromosomes into two new identical daughter cells. To achieve this and maintain the correct amount of
deoxyribo nuclic acid
(DNA) in the cells, the cell forms a framework called the mitotic spindle onto which the chromosomes attach and then get pulled into the new daughter cells. The mitotic spindle is made up of microtubules and associated proteins. The GTPase Ran, which is important for nuclear import and export, plays imp… Show more
“…Ran is involved in mitotic spindle assembly, nuclear envelope assembly, chromosome segregation, and processes occurring during anaphase and cytokinesis (Joseph et al 2002;reviewed in Quimby and Dasso 2003;Renshaw and Wilde 2011;Figure 8). RanGAP and RanGEF are critical in establishing the gradient of Ran-GDP and Ran-GTP for these other cellular functions and not only across the nuclear envelope ( Figure 8A).…”
Segregation Distorter (SD) is an autosomal meiotic drive gene complex found worldwide in natural populations of Drosophila melanogaster. During spermatogenesis, SD induces dysfunction of SD + spermatids so that SD/SD + males sire almost exclusively SD-bearing progeny rather than the expected 1:1 Mendelian ratio. SD is thus evolutionarily "selfish," enhancing its own transmission at the expense of its bearers. Here we review the molecular and evolutionary genetics of SD. Genetic analyses show that the SD is a multilocus gene complex involving two key loci-the driver, Segregation distorter (Sd), and the target of drive, Responder (Rsp)-and at least three upward modifiers of distortion. Molecular analyses show that Sd encodes a truncated duplication of the gene RanGAP, whereas Rsp is a large pericentromeric block of satellite DNA. The Sd-RanGAP protein is enzymatically wild type but mislocalized within cells and, for reasons that remain unclear, appears to disrupt the histone-to-protamine transition in drive-sensitive spermatids bearing many Rsp satellite repeats but not drive-insensitive spermatids bearing few or no Rsp satellite repeats. Evolutionary analyses show that the Sd-RanGAP duplication arose recently within the D. melanogaster lineage, exploiting the preexisting and considerably older Rsp satellite locus. Once established, the SD haplotype collected enhancers of distortion and suppressors of recombination. Further dissection of the molecular genetic and cellular basis of SD-mediated distortion seems likely to provide insights into several important areas currently understudied, including the genetic control of spermatogenesis, the maintenance and evolution of satellite DNAs, the possible roles of small interfering RNAs in the germline, and the molecular population genetics of the interaction of genetic linkage and natural selection.Mendelian inheritance is a marvelous device for making evolution by natural selection an efficient process.... The Mendelian system works with maximum efficiency only if it is scrupulously fair to all genes. It is in constant danger, however, of being upset by genes that subvert the meiotic process to their own advantage. James F. Crow (1979) S EGREGATION Distorter (SD) is a selfish, coadapted gene complex on chromosome 2 (an autosome) found at low frequency in nearly all natural populations of the fruit fly, Drosophila melanogaster. In heterozygous males carrying SD and a typical wild-type second chromosome (SD/SD + ), most SD + -bearing spermatid nuclei fail to complete the histoneto-protamine transition during spermiogenesis, so that primarily SD-bearing spermatids develop properly and go on to fertilize eggs. SD/SD + males thus sire almost exclusively SD-inheriting progeny. This distortion of classic Mendelian ratios has intrigued geneticists and evolutionary biologists for more than 50 years-and for good reason. As we describe below, SD is a newly evolved system that subverts one of the fundamental laws of inheritance by exploiting an ancient molecular pathway. I...
“…Ran is involved in mitotic spindle assembly, nuclear envelope assembly, chromosome segregation, and processes occurring during anaphase and cytokinesis (Joseph et al 2002;reviewed in Quimby and Dasso 2003;Renshaw and Wilde 2011;Figure 8). RanGAP and RanGEF are critical in establishing the gradient of Ran-GDP and Ran-GTP for these other cellular functions and not only across the nuclear envelope ( Figure 8A).…”
Segregation Distorter (SD) is an autosomal meiotic drive gene complex found worldwide in natural populations of Drosophila melanogaster. During spermatogenesis, SD induces dysfunction of SD + spermatids so that SD/SD + males sire almost exclusively SD-bearing progeny rather than the expected 1:1 Mendelian ratio. SD is thus evolutionarily "selfish," enhancing its own transmission at the expense of its bearers. Here we review the molecular and evolutionary genetics of SD. Genetic analyses show that the SD is a multilocus gene complex involving two key loci-the driver, Segregation distorter (Sd), and the target of drive, Responder (Rsp)-and at least three upward modifiers of distortion. Molecular analyses show that Sd encodes a truncated duplication of the gene RanGAP, whereas Rsp is a large pericentromeric block of satellite DNA. The Sd-RanGAP protein is enzymatically wild type but mislocalized within cells and, for reasons that remain unclear, appears to disrupt the histone-to-protamine transition in drive-sensitive spermatids bearing many Rsp satellite repeats but not drive-insensitive spermatids bearing few or no Rsp satellite repeats. Evolutionary analyses show that the Sd-RanGAP duplication arose recently within the D. melanogaster lineage, exploiting the preexisting and considerably older Rsp satellite locus. Once established, the SD haplotype collected enhancers of distortion and suppressors of recombination. Further dissection of the molecular genetic and cellular basis of SD-mediated distortion seems likely to provide insights into several important areas currently understudied, including the genetic control of spermatogenesis, the maintenance and evolution of satellite DNAs, the possible roles of small interfering RNAs in the germline, and the molecular population genetics of the interaction of genetic linkage and natural selection.Mendelian inheritance is a marvelous device for making evolution by natural selection an efficient process.... The Mendelian system works with maximum efficiency only if it is scrupulously fair to all genes. It is in constant danger, however, of being upset by genes that subvert the meiotic process to their own advantage. James F. Crow (1979) S EGREGATION Distorter (SD) is a selfish, coadapted gene complex on chromosome 2 (an autosome) found at low frequency in nearly all natural populations of the fruit fly, Drosophila melanogaster. In heterozygous males carrying SD and a typical wild-type second chromosome (SD/SD + ), most SD + -bearing spermatid nuclei fail to complete the histoneto-protamine transition during spermiogenesis, so that primarily SD-bearing spermatids develop properly and go on to fertilize eggs. SD/SD + males thus sire almost exclusively SD-inheriting progeny. This distortion of classic Mendelian ratios has intrigued geneticists and evolutionary biologists for more than 50 years-and for good reason. As we describe below, SD is a newly evolved system that subverts one of the fundamental laws of inheritance by exploiting an ancient molecular pathway. I...
Segregation distorter (SD) is a naturally occurring male meiotic drive system in Drosophila melanogaster characterized by almost exclusive transmission of the SD chromosome owing to dysfunction of sperm receiving the SD+ homologue. Previous studies identified at least three closely linked loci on chromosome 2 required for distortion: Sd, the primary distorting gene; E(SD), Enhancer, which increases the strength of distortion; and Rsp (Responder), the apparent target of Sd. Strength of distortion is also influenced by linked upwards modifiers including M(SD), Modifier, and St(SD), Stabilizer, and by various unlinked suppressors. Although Sd is known to encode a mutant RanGAP protein none of the modifiers have been molecularly identified. This work focuses on the genetic and cytological characterization of a strong X-linked suppressor, Su(SD), capable of restoring Mendelian transmission in SD/SD+ males. Sd and its cohort of positive modifiers appear to act semi-quantitatively in opposition to Su(SD) with distortion strength depending primarily on the total number of distorting elements rather than which particular elements are present. Su(SD) can also suppress male sterility observed in certain SD genotypes. To facilitate its eventual molecular identification, Su(SD) was localized by deletion mapping to polytene region 13C7-13E4. These studies highlight the polygenic nature of distortion and its dependence on a constellation of positive and negative modifiers, they provide insight into the stability of Mendelian transmission in natural populations even when a drive system arises, and they pave the way for molecular characterization of Su(SD) whose identity should reveal new information about the mechanism of distortion.
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