Literature DB >> 17246219

Factors Influencing the Effect of Segregation Distortion in Natural Populations of DROSOPHILA MELANOGASTER.

R G Temin1, M Marthas.   

Abstract

The major components of the SD system have been examined in two natural populations of D. melanogaster to investigate how SD behaves and is maintained in nature and to estimate its impact and efficiency. A twofold approach was used: (1) direct measurements of segregation distortion in wild males and (2) measurement of sensitivity of wild SD (+) chromosomes to SD action. Characterization of newly isolated SD chromosomes and of a large number of SD( +) chromosomes from nature demonstrated that (1) SD can operate efficiently in the wild genome: 45% of SD/SD(+) males collected from nature had k values larger than 0.70. (2) Forty-three of 44 newly recovered SD chromosomes are of the SD-72 type, having a small pericentric inversion that maintains tight linkage among the Sd, E(SD) and Rsp loci in the SD complex. In 1956, most SD chromosomes in Madison lacked this inversion. (3) Only 12 of the 44 SD chromosomes carried a recessive lethal (compared with five of six in 1956), and many of the viable SD chromosomes were fertile as homozygotes, indicating that SD homozygotes need not have obvious reductions in fitness. (4) Among more than 500 wild chromosomes assayed for response to distortion by a strong SD, at least 40-50% were sensitive, about 33% were partially sensitive and 17% were insensitive. This frequency of sensitives is higher than in reports from some other populations. An estimated 12% of the wild chromosomes were classified as true Rsp(i) by their constellation of effects, including a special test of ability to cause self-distortion of a "suicide" chromosome, R(cn)-10. In a direct assay with R(cn)-10, an independent sample of 99 chromosomes from nature gave 30% putative Rsp(i). Thus, these populations contain in the range of 12-30% Rsp(i). (5) Chromosomes supersensitive to SD, previously described for certain laboratory stocks, were also found to coexist in nature with SD. (6) Profiles of wild chromosomes with a panel of three or four different SD testers suggest a series of allelic alternatives at the Rsp locus including supersensitive, sensitive, semisensitive and insensitive, and that loci other than Rsp may also be important in determining the effect of SD in nature.

Entities:  

Year:  1984        PMID: 17246219      PMCID: PMC1202330     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  5 in total

1.  Population genetics of modifiers of meiotic drive. I. The solution of a special case and some general implications.

Authors:  T Prout; J Bundgaard; S Bryant
Journal:  Theor Popul Biol       Date:  1973-12       Impact factor: 1.570

2.  Evidence for sperm dysfunction as the mechanism of segregation distortion in Drosophila melanogaster.

Authors:  D L Hartl; Y Hiraizumi; J F Crow
Journal:  Proc Natl Acad Sci U S A       Date:  1967-12       Impact factor: 11.205

3.  On the Models of Segregation Distortion in DROSOPHILA MELANOGASTER.

Authors:  D W Martin; Y Hiraizumi
Journal:  Genetics       Date:  1979-10       Impact factor: 4.562

4.  An investigation of the components of Segregation-Distorter systems in Drosophila melanogaster.

Authors:  G L Miklos
Journal:  Genetics       Date:  1972-03       Impact factor: 4.562

5.  Deviant sex ratio associated with segregation distortion in Drosophila melanogaster.

Authors:  Y Hiraizumi; K Nakazima
Journal:  Genetics       Date:  1967-04       Impact factor: 4.562

  5 in total
  28 in total

1.  The segregation distortion (SD) phenomenon in wild populations of Drosophila melanogaster: interaction between chromosomes 3 and SD chromosomes 2.

Authors:  R Cicchetti; G Argentin; B Nicoletti
Journal:  Genetica       Date:  1990       Impact factor: 1.082

2.  Detection of Rsp and modifier variation in the meiotic drive system Segregation distorter (SD) of Drosophila melanogaster.

Authors:  T W Lyttle; J G Brittnacher; B Ganetzky
Journal:  Genetics       Date:  1986-09       Impact factor: 4.562

3.  Causes of sex ratio bias may account for unisexual sterility in hybrids: a new explanation of Haldane's rule and related phenomena.

Authors:  L D Hurst; A Pomiankowski
Journal:  Genetics       Date:  1991-08       Impact factor: 4.562

4.  Rapid evolution of a coadapted gene complex: evidence from the Segregation Distorter (SD) system of meiotic drive in Drosophila melanogaster.

Authors:  M F Palopoli; C I Wu
Journal:  Genetics       Date:  1996-08       Impact factor: 4.562

5.  Segregation distortion in Drosophila melanogaster: genomic organization of Responder sequences.

Authors:  R Moschetti; R Caizzi; S Pimpinelli
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

6.  Cytogenetic analysis of segregation distortion in Drosophila melanogaster: the cytological organization of the Responder (Rsp) locus.

Authors:  S Pimpinelli; P Dimitri
Journal:  Genetics       Date:  1989-04       Impact factor: 4.562

7.  Origin, evolution, and population genetics of the selfish Segregation Distorter gene duplication in European and African populations of Drosophila melanogaster.

Authors:  Cara L Brand; Amanda M Larracuente; Daven C Presgraves
Journal:  Evolution       Date:  2015-04-29       Impact factor: 3.694

8.  On the components of segregation distortion in Drosophila melanogaster. V. Molecular analysis of the Sd locus.

Authors:  P A Powers; B Ganetzky
Journal:  Genetics       Date:  1991-09       Impact factor: 4.562

9.  The independent distorting ability of the Enhancer of Segregation Distortion, E(SD), in Drosophila melanogaster.

Authors:  R G Temin
Journal:  Genetics       Date:  1991-06       Impact factor: 4.562

Review 10.  The selfish Segregation Distorter gene complex of Drosophila melanogaster.

Authors:  Amanda M Larracuente; Daven C Presgraves
Journal:  Genetics       Date:  2012-09       Impact factor: 4.562

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