scholarly journals FERTILITY GENES IN NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER. I. FREQUENCY, ALLELISM AND PERSISTENCE OF STERILITY GENES

Genetics ◽  
1973 ◽  
Vol 74 (2) ◽  
pp. 351-361
Author(s):  
Chozo Oshima ◽  
Takao K Watanabe
Keyword(s):  
Natural Populations ◽  
Pleiotropic Effect ◽  
Female Sterility ◽  
Male And Female ◽  
Random Combination ◽  
Cage Population ◽  
Male And Female Sterility ◽  
Fertility Genes ◽  
Sterility Genes ◽  
Lethal Genes

ABSTRACT Three or four percent of the wild flies in natural populations of D. melanogaster have been found to be sterile. An analysis of sterility associated with the second chromosome revealed a much lower frequency of genetically sterile flies. The accumulation of sterility genes in a cage population was proportional to that of lethal genes, as were their equilibrium frequencies in several natural populations. Many sterile chromosomes were associated with low viability due to pleiotropic effects. The number of chromosomes leading to sterility in both sexes was larger than the expectation based on random combination of male and female sterility genes. This suggests that there is some linkage disequilibrium between male and female sterility genes, as well as a pleiotropic effect of single sterility genes. Some sterility genes were maintained in natural and cage populations, and the patterns of persistence of the sterility genes were very similar to those of lethal genes.

Drosophila melanogaster Importin α1 and α3 Can Replace Importin α2 During Spermatogenesis but Not Oogenesis

Genetics ◽  
2002 ◽  
Vol 161 (1) ◽  
pp. 157-170 ◽  
Author(s):  
D Adam Mason ◽  
Robert J Fleming ◽  
David S Goldfarb
Keyword(s):  
Drosophila Melanogaster ◽  
Female Sterility ◽  
Degenerate Pcr ◽  
Male And Female ◽  
Importin Α ◽  
Localization Signal ◽  
Male And Female Sterility ◽  
A Site ◽  
Female Gametogenesis

Abstract Importin α’s mediate the nuclear transport of many classical nuclear localization signal (cNLS)-containing proteins. Multicellular animals contain multiple importin α genes, most of which fall into three conventional phylogenetic clades, here designated α1, α2, and α3. Using degenerate PCR we cloned Drosophila melanogaster importin α1, α2, and α3 genes, demonstrating that the complete conventional importin α gene family arose prior to the split between invertebrates and vertebrates. We have begun to analyze the genetic interactions among conventional importin α genes by studying their capacity to rescue the male and female sterility of importin α2 null flies. The sterility of α2 null males was rescued to similar extents by importin α1, α2, and α3 transgenes, suggesting that all three conventional importin α’s are capable of performing the important role of importin α2 during spermatogenesis. In contrast, sterility of α2 null females was rescued only by importin α2 transgenes, suggesting that it plays a paralog-specific role in oogenesis. Female infertility was also rescued by a mutant importin α2 transgene lacking a site that is normally phosphorylated in ovaries. These rescue experiments suggest that male and female gametogenesis have distinct requirements for importin α2.

Aberrant microspore development in hybrids of maize × Tripsacum dactyloides

Genome ◽  
1993 ◽  
Vol 36 (5) ◽  
pp. 987-997 ◽  
Author(s):  
Bryan Kindiger
Keyword(s):  
Pollen Development ◽  
Cytological Study ◽  
Metaphase Plate ◽  
Pollen Grains ◽  
Female Sterility ◽  
Microspore Development ◽  
Tripsacum Dactyloides ◽  
Male And Female ◽  
Inherent Problem ◽  
Male And Female Sterility

Cytogenetic investigations of meiosis in hybrids between maize and Tripsacum have been well documented; however, the inherent problem of male and female sterility has not been addressed either on a genetic or cytogenetic level. The purpose of this cytological study was to identify some of the probable causes of male sterility in maize × Tripsacum dactyloides hybrids. Disturbances in pollen development of maize × T. dactyloides hybrids, derived from both diploid (2n) and tetraploid (4n) Tripsacum sources, were commonly observed. Anomalies in the development of the microspore apparently occurred because of a failure of the chromosomes to congregate at the metaphase plate, development of a tripolar spindle, and failure of cytokinesis at the first and second meiotic divisions. Phenotypic features of abnormal microspore development were the maturation of large pollen grains, "Siamese" pollen grains, the occurrence of variable invaginations, and a nuclear budding-type behavior. These abnormalities were not observed in the 56-chromosome amphidiploid or the 38-chromosome backcross generations.Key words: maize, Tripsacum, microspore, sterility.

scholarly journals Sterile mutation in Drosophila melanogaster

1977 ◽  
Vol 30 (2) ◽  
pp. 107-113 ◽  
Author(s):  
Takao K. Watanabe ◽  
Won Ho Lee
Keyword(s):  
Drosophila Melanogaster ◽  
Male Sterility ◽  
Female Sterility ◽  
Sterility Genes ◽  
Lethal Genes

SUMMARYThe number of loci which are potentially able to produce sterility genes was estimated for Drosophila melanogaster. There appear to be, on the second chromosome, about 80 loci capable of producing male sterility and about 60 loci capable of producing female sterility. These figures seem to be considerably less than (400–500) loci responsible for lethal genes.

scholarly journals Male and female sterility in Zambia

2014 ◽  
Vol 30 ◽  
pp. 413-428
Author(s):  
Athena Pantazis ◽  
Samuel J. Clark
Keyword(s):  
Female Sterility ◽  
Male And Female ◽  
Male And Female Sterility

Molecular mapping of five soybean genes involved in male-sterility, female-sterility

Genome ◽  
2015 ◽  
Vol 58 (4) ◽  
pp. 143-149 ◽  
Author(s):  
Benjamin Speth ◽  
Joshua P. Rogers ◽  
Napatsakorn Boonyoo ◽  
A.J. VanMeter ◽  
Jordan Baumbach ◽  
...  
Keyword(s):  
Molecular Mapping ◽  
Female Sterility ◽  
Chromosome 11 ◽  
Male Sterile ◽  
Sterile Female ◽  
Fertility Reduction ◽  
And Function ◽  
Fertility Genes ◽  
Sterility Genes

In soybean, asynaptic and desynaptic mutants lead to abnormal meiosis and fertility reduction. Several male-sterile, female-sterile mutants have been identified and studied in soybean, however, some of these mutants have not been mapped to locations on soybean chromosomes. The objectives of this study were to molecularly map five male-sterile, female-sterile genes (st2, st4, st5, st6, and st7) in soybean and compare the map locations of these genes with already mapped sterility genes. Microsatellite markers were used in bulked segregant analyses to locate all five male-sterile, female-sterile genes to soybean chromosomes, and markers from the corresponding chromosomes were used on F2 populations to generate genetic linkage maps. The st2, st4, st5, st6, and st7 genes were located on molecular linkage group (MLG) B1 (chromosome 11), MLG D1a (chromosome 01), MLG F (chromosome 13), MLG B2 (chromosome 14), and D1b (chromosome 02), respectively. The st2, st4, st5, st6, and st7 genes were flanked to 10.3 (∼399 kb), 6.3 (∼164 kb), 3.9 (∼11.8 Mb), 11.0 (∼409 kb), and 5.3 cM (∼224 kb), and the flanked regions contained 57, 17, 362, 52, and 17 predicted genes, respectively. Future characterization of candidate genes should facilitate identification of the male- and female-fertility genes, which may provide vital insights on structure and function of genes involved in the reproductive pathway in soybean.

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