scholarly journals X-linked elements associated with negative segregation distortion in the SD system of Drosophila melanogaster.

Genetics ◽  
1994 ◽  
Vol 138 (1) ◽  
pp. 145-152
Author(s):  
Y Hiraizumi ◽  
J M Albracht ◽  
B C Albracht
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Segregation Distortion ◽  
Recovery Rate ◽  
Considerable Decrease ◽  
Negative Segregation ◽  
The Third ◽  
Switch Mechanism ◽  
Rate Of Recovery

Abstract Three elements, M1, M2 and M3, found in a special X chromosome, supp-X(SD), modify the degree and direction of segregation distortion in the SD system of Drosophila melanogaster. The first element, M1, is located between the y and the cv loci, probably close to the y locus. The second element, M2, is located near the cv locus and the third element, M3, is located between the y and the car loci. The M1 element appears to cause a relatively small amount of reduction in the rate of recovery of the SD-72, but not the cn bw, chromosome from SD-72/cn bw males, when raised at 27.5 degrees. The M2 and the M3 elements cause considerable decrease in the recovery rate of the SD-72 chromosome, whereas they increase the recovery rate of the cn bw chromosome. The amount of decrease is nearly the same as the amount of increase for each element. Some type of "switch" mechanism in the directions of distortion is suggested for each of these two elements and their effects appear to be approximately additive.

scholarly journals Temperature sensitivity of negative segregation distortion in Drosophila melanogaster.

Genetics ◽  
1993 ◽  
Vol 135 (3) ◽  
pp. 831-841 ◽  
Author(s):  
Y Hiraizumi
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Segregation Distortion ◽  
Current Model ◽  
Sensitive Period ◽  
Temperature Sensitive ◽  
Absolute Increase ◽  
Negative Segregation ◽  
Absolute Reduction ◽  
Radical Revision

Abstract Previous work has shown that the direction of segregation distortion in the SD (Segregation Distorter) system in Drosophila melanogaster can sometimes be reversed, but this was found only with rather weak distorters and the effect was not large. The present study reports large negative segregation distortion in a strong distorter, SD-72 chromosome. In the presence of a specific X chromosome, supp-X(SD), the proportion, k, of SD-72 chromosomes recovered from the SD-72/cn bw males ranges from 0.99 at 20 degrees to 0.11 at 28.5 degrees, whereas with a standard-X chromosome, k ranges from 0.99 to 0.95 for the same temperature range. The temperature-sensitive period is during spermiogenesis. Using a mating system in which the sperm supply is nearly exhausted, it was shown that the negative distortion at high temperatures is due to an absolute reduction in the number of SD-72 chromosomes and an absolute increase in the number of cn bw chromosomes recovered. After adjusting for non-SD-related temperature effects, the amount of decrease in the number of SD-72 progeny is nearly the same as the amount of increase in the number of cn bw progeny, suggesting that the dysfunction switches from a spermatid carrying one homolog to one carrying the other. Negative distortion requires a radical revision of current hypotheses for the mechanism of segregation distortion and a possible modification of the current model is suggested, based on differential recovery of dysfunction in the two homologs during spermiogenesis.

scholarly journals Negative segregation distortion in the SD system of Drosophila melanogaster: a challenge to the concept of differential sensitivity of Rsp alleles.

Genetics ◽  
1990 ◽  
Vol 125 (3) ◽  
pp. 515-525
Author(s):  
Y Hiraizumi
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Segregation Distortion ◽  
Experimental Results ◽  
Differential Sensitivity ◽  
Female Transfer ◽  
New Model ◽  
Young Males ◽  
Negative Segregation

Abstract Current models of segregation distortion based on previous experimental results predict that, in the Sd heterozygous Rspi/Rsps male, the chromosome carrying the sensitive Rsps allele is distorted or transmitted in a frequency smaller than that of the expected Mendelian 0.5 relative to the chromosome carrying the insensitive Rspi allele. The present study presents a case where this does not occur, that is, when the genotype of the males is supp-X(SD)/Y; Sd E(SD)Rspi M(SD)+/Sd+ E(SD)+ Rsps M(SD)+ where supp-X(SD) is an X chromosome carrying a strong suppressor or suppressors of SD activity and SD+ E(SD)+ Rsps M(SD)+ is the standard cn bw chromosome. Following the "inseminated female transfer" procedure, young males of the above genotype carrying the standard-X instead of the supp-X(SD) chromosome show k values for the SD chromosome (frequencies of the SD chromosome recovered among progeny) of about 0.75, but with the supp-X(SD) chromosome, the k values are reduced to 0.36-0.41. Several possibilities other than the mechanism of segregation distortion to explain the reduced k values are ruled out. The occurrence of "negative segregation distortion" is clearly demonstrated, where the chromosome carrying the Rspi allele is distorted but the chromosome with the Rsps allele is not. This result requires a major modification of the current models or even a new model for the mechanism of segregation distortion to accommodate Rsp allele sensitivity or insensitivity. The present study also shows that males of the genotype, Sd Rspss M(SD)+/Sd+ Rspss M(SD), are almost completely sterile, but their fertility is considerably increased when SD activity is suppressed by the presence of the supp-X(SD) chromosome. This result suggests that the amount of the Sd product is not limited with respect to the interacting sites available, that is, the amount is large enough to interact with both of the Rspss alleles.

scholarly journals Studies of esterase 6 in Drosophila melanogaster: XIV. Variation of esterase 6 levels controlled by unlinked genes in natural populations

1984 ◽  
Vol 43 (2) ◽  
pp. 181-190 ◽  
Author(s):  
Craig S. Tepper ◽  
Anne L. Terry ◽  
James E. Holmes ◽  
Rollin C. Richmond
Keyword(s):  
Drosophila Melanogaster ◽  
Structural Gene ◽  
X Chromosome ◽  
Genetic Background ◽  
Natural Populations ◽  
Regulatory Elements ◽  
Regulatory Locus ◽  
The Third ◽  
Esterase 6 ◽  
Activity Modifiers

SUMMARYThe esterase 6 (Est-6) locus in Drosophila melanogaster is located on the third chromosome and is the structural gene for a carboxylesterase (E.C.3.1.1.1) and is polymorphic for two major electromorphs (slow and fast). Isogenic lines containing X chromosomes extracted from natural populations and substituted into a common genetic background were used to detect unlinked factors that affect the activity of the Est-6 locus. Twofold activity differences of esterase 6 (EST 6) were found among males from these derived lines, which differ only in their X chromosome. These unlinked activity modifiers identify possible regulatory elements. Immunoelectrophoresis was used to estimate quantitatively the levels of specific cross-reacting material in the derived lines. The results show that the variation in activity is due to differences in the amount of EST 6 present. The data are consistent with the hypothesis that there is at least one locus on the X chromosome that regulates the synthesis of EST 6 and that this regulatory locus may be polymorphic in natural populations.

scholarly journals Interactions and developmental effects of mutations in the Broad-Complex of Drosophila melanogaster.

Genetics ◽  
1988 ◽  
Vol 118 (2) ◽  
pp. 247-259
Author(s):  
I Kiss ◽  
A H Beaton ◽  
J Tardiff ◽  
D Fristrom ◽  
J W Fristrom
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Genetic Locus ◽  
Larval Instar ◽  
Imaginal Discs ◽  
Functional Domains ◽  
Developmental Processes ◽  
The Third ◽  
Developmental Effects ◽  
Broad Complex

Abstract The 2B5 region on the X chromosome of Drosophila melanogaster forms an early ecdysone puff at the end of the third larval instar. The region contains a complex genetic locus, the Broad-Complex (BR-C) composed of four groups of fully complementing (br, rbp, l(1)2Bc, and l(1)2Bd) alleles, and classes of noncomplementing (npr 1) and partially noncomplementing l(1)2Bab alleles. BR-C mutants prevent metamorphosis, including the morphogenesis of imaginal discs. Results are presented that indicate that the BR-C contains two major functional domains. One, the br domain is primarily, if not exclusively, involved in the elongation and eversion of appendages by imaginal discs. The second, the l(1)2Bc domain, is primarily involved in the fusion of discs to form a continuous adult epidermis. Nonetheless, the two domains may encode products with related functions because in some situations mutants in both domains appear to affect similar developmental processes.

scholarly journals Examination of a mutable system affecting the components of the segregation distorter meiotic drive system of Drosophila melanogaster.

Genetics ◽  
1990 ◽  
Vol 125 (1) ◽  
pp. 51-76
Author(s):  
K G Golic
Keyword(s):  
Drosophila Melanogaster ◽  
Transposable Element ◽  
X Chromosome ◽  
Segregation Distortion ◽  
Chromosomal Rearrangements ◽  
Meiotic Drive ◽  
Drive System ◽  
Partial Loss ◽  
Segregation Distorter ◽  
Relationship Of

Abstract Segregation distortion in Drosophila melanogaster is the result of an interaction between the genetic elements Sd, a Rsp sensitive to Sd, and an array of modifiers, that results in the death of sperm carrying Rsp. A stock (designated M-5; cn bw) has been constructed which has the property of inducing the partial loss of sensitivity from previously sensitive cn bw chromosomes, the partial loss of distorting ability from SD chromosomes, and a concomitant acquisition of modifiers on the X chromosome and possibly also on the autosomes. By several criteria the changes exhibited under the influence of M-5; cn bw are characteristic of the transposable-element systems which produce hybrid dysgenesis. In the first place, the magnitude of these effects depends on the nature of the crosses performed. The analogy is further strengthened by the observation that the changes induced by M-5; cn bw share other stigmata of Drosophila transposable-element systems, including high sterility among the progeny of outcrosses, and the production of chromosomal rearrangements. The possible relationship of this system to the P, I and hobo transposable element systems is discussed, as well as its bearing on aspects of the Segregation Distorter phenomenon which have yet to be explained.

Requirements for autosomal gene activity during precellular stages of Drosophila melanogaster

Development ◽  
1988 ◽  
Vol 104 (3) ◽  
pp. 495-509 ◽  
Author(s):  
P.T. Merrill ◽  
D. Sweeton ◽  
E. Wieschaus
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Single Cells ◽  
Gene Activity ◽  
Autosomal Gene ◽  
The Third ◽  
Specific Effects ◽  
Morphological Defects ◽  
Zygotic Gene

To identify early requirements for zygotic gene activity in Drosophila, we used compound autosomes and autosome-Y translocations to generate embryos deficient for cytologically defined portions of the genome. No obvious gross morphological defects were observed in any deficiency class until the beginning of cycle 14. Only seven autosomal regions were identified with discrete effects visible prior to the onset of gastrulation. These regions include genes with locus-specific effects on the clearing of the cortical cytoplasm during early cycle 14, (22AB), the initiation of the slow and fast phases of cellularization (26BF and 40AC, respectively), the apical-basal distribution of nuclei during cycle 14 (71C-75C) and the closing off of furrow canals during cellularization (100AC). The distal tip of the third chromosome also contains two loci (99DF and 100AC) whose deletion causes multiple nuclei to be cellularized into single cells, a phenotype similar to that produced in embryos totally lacking the X-chromosome.

MALELESS, A RECESSIVE AUTOSOMAL MUTANT OF DROSOPHILA MELANOGASTER THAT SPECIFICALLY KILLS MALE ZYGOTES

Genetics ◽  
1975 ◽  
Vol 81 (1) ◽  
pp. 135-141
Author(s):  
Akihiro Fukunaga ◽  
Atsumi Tanaka ◽  
Kugao Oishi
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Larval Stage ◽  
Lethal Gene ◽  
Homozygous Condition ◽  
The Third ◽  
Male Specific Lethal ◽  
Male Specific ◽  
Transforming Genes

ABSTRACT A second chromosome male-specific lethal gene, maleless (mle), in D. melanogaster is described. It kills males but not females in homozygous condition, regardless of whether female parents are heterozygous or homozygous for mle. Many, if not most, homozygous males survive up to the third instar larval stage, but cannot pupate and die eventually as larvae. No interactions with sex-transforming genes, tra and dsx, were observed. It is proposed that mle interacts with a gene(s) on the X chromosome, which is not dosage compensated.

scholarly journals A CYTOGENETIC ANALYSIS OF CYCLIC NUCLEOTIDE PHOSPHODIESTERASE ACTIVITIES IN DROSOPHILA

Genetics ◽  
1977 ◽  
Vol 85 (4) ◽  
pp. 609-622
Author(s):  
John A Kiger ◽  
Eric Golanty
Keyword(s):  
Drosophila Melanogaster ◽  
Structural Gene ◽  
X Chromosome ◽  
Cyclic Nucleotide ◽  
Phosphodiesterase Activity ◽  
Structural Genes ◽  
Camp Phosphodiesterase ◽  
Cgmp Phosphodiesterase ◽  
The Third ◽  
Segmental Aneuploidy

ABSTRACT The genome of Drosophila melanogaster has been surveyed for chromosomal regions which exert a dosage effect on the activities of cAMP phosphodiesterase or cGMP phosphodiesterase. Two regions increase cAMP phosphodiesterase activity when present as duplications. A region of the X chromosome increases cAMP phosphodiesterase activity when duplicated and decreases that activity when deficient. This region has been delimited to chromomeres 3D3 and 3D4, with 3D4 being the most probable locus, and may contain a structural gene for cAMP phosphodiesterase. A region on the third chromosome, 90E-91B, increase cAMP phosphodiesterase activity when duplicated but has no affect on the activity when deficient. Two regions increase cGMP phosphodiesterase activity when present as duplications. A region of the X chromosome, 5D-9C, increases cGMP phosphodiesterase activity when duplicated, but smaller duplications covering this region fail to show such an increase, indicating that a single locus is not responsible for the increase observed for the larger duplication. A region of the third chromosome, 88C-91B, also increases cGMP phosphodiesterase activity when duplicated. Smaller duplications covering this region show smaller increases than that observed for the larger duplication, suggesting that at least three loci between 88C and 91B contribute to the observed increase by that region. Deficiencies covering region 88C-91B do not affect cGMP phosphodiesterase activity. No locus for a presumptive structural gene for cGMP phosphodiesterase has been found. Limitations of the use of segmental aneuploidy in locating structural genes for enzymes are discussed.

scholarly journals Suppression of a lethal trisomic phenotype in Drosophila melanogaster by increased dosage of an unlinked locus.

Genetics ◽  
1993 ◽  
Vol 134 (1) ◽  
pp. 243-249 ◽  
Author(s):  
D R Dorer ◽  
M A Cadden ◽  
B Gordesky-Gold ◽  
G Harries ◽  
A C Christensen
Keyword(s):  
Drosophila Melanogaster ◽  
X Chromosome ◽  
Gene Dosage ◽  
Chromosome Region ◽  
Dosage Effect ◽  
Gene Dosage Effect ◽  
Unlinked Locus ◽  
Lethal Phenotype ◽  
The Third ◽  
Dosage Sensitivity

Abstract One of the most extreme examples of gene dosage sensitivity is the Triplo-lethal locus (Tpl) on the third chromosome of Drosophila melanogaster, which is lethal when present in either one or three copies. Increased dosage of an unlinked locus, Isis, suppresses the triplo-lethal phenotype of Tpl, but not the haplo-lethal phenotype. We have mapped Isis to the X chromosome region 7E3-8A5, and shown that the suppression is a gene dosage effect. Altered dosage of Isis in the presence of two copies of Tpl has no obvious effects. By examining the interactions between Isis dosage and Tpl we suggest that Isis does not directly repress Tpl expression, but acts downstream on the triplo-lethal phenotype of Tpl.

scholarly journals A possible case of negative segregation distortion in the SD system of Drosophila melanogaster.

Genetics ◽  
1989 ◽  
Vol 121 (2) ◽  
pp. 263-271
Author(s):  
Y Hiraizumi
Keyword(s):  
Drosophila Melanogaster ◽  
Segregation Distortion ◽  
Relative Sensitivity ◽  
New Model ◽  
Negative Segregation ◽  
The One

Abstract Models proposed to explain segregation distortion in Drosophila melanogaster are based partly upon the observation that, in the Sd heterozygous Rspi/Rsps male, the chromosome carrying the sensitive Rsps allele is distorted, but the chromosome carrying the insensitive Rspi allele is not. The results of the present study suggest that this may not always be the case. Under a certain genotypic condition, the chromosome carrying the Rsps allele can be transmitted to the progeny in frequencies of more than 0.5 (about 0.6), or correspondingly, the chromosome carrying the Rspi allele may be distorted with respect to the one with the Rsps allele. Thus, the relative sensitivity and insensitivity of the two Rsp alleles in a male are not absolute, but relative; and they may be reversed depending upon the residual genotype. If this is true, a major modification of the current models or a proposal of an entirely new model may become necessary to explain the mechanism of segregation distortion satisfactorily.

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