Major Differences in the Frequencies of Radiation-Induced Malformations and Eye Color Mutants in Mature Oocytes of the Wasp Dahlbominus

1975 ◽  
Vol 63 (2) ◽  
pp. 320
Author(s):  
W. F. Baldwin ◽  
P. A. Knight

1968 ◽  
Vol 23 (3) ◽  
pp. 376-386 ◽  
Author(s):  
Armin Wessing ◽  
Dieter Eichelberg

The Malpighian tubules of Drosophila melanogaster accumulate a great number of substances, many of which fluoresce. This paper is concerned with the identification of these substances by chromatography and their location by fluorescentmicroscopy (fig. 4, 5). It appears that they mainly belong to the following three groups: Pteridines, tryptophane and some of its metabolites, and riboflavine (tab. 1).The pattern of fluorescent substances of the eye color mutants cn, v, se, st, bw, ry, and w vary significantly. The patterns of these mutants are compared and discussed with that of the wild-type.



Genetics ◽  
1989 ◽  
Vol 123 (3) ◽  
pp. 511-524 ◽  
Author(s):  
W Sequeira ◽  
C R Nelson ◽  
P Szauter

Abstract The claret (ca) locus of Drosophila melanogaster comprises two separately mutable domains, one responsible for eye color and one responsible for proper disjunction of chromosomes in meiosis and early cleavage divisions. Previously isolated alleles are of three types: (1) alleles of the claret (ca) type that affect eye color only, (2) alleles of the claret-nondisjunctional (cand) type that affect eye color and chromosome behavior, and (3) a meiotic mutation, non-claret disjunctional (ncd), that affects chromosome behavior only. In order to investigate the genetic structure of the claret locus, we have isolated 19 radiation-induced alleles of claret on the basis of the eye color phenotype. Two of these 19 new alleles are of the cand type, while 17 are of the ca type, demonstrating that the two domains do not often act as a single target for mutagenesis. This suggests that the two separately mutable functions are likely to be encoded by separate or overlapping genes rather than by a single gene. One of the new alleles of the cand type is a chromosome rearrangement with a breakpoint at the position of the claret locus. If this breakpoint is the cause of the mutant phenotype and there are no other mutations associated with the rearrangement, the two functions must be encoded by overlapping genes.



1979 ◽  
Vol 17 (5-6) ◽  
pp. 565-573 ◽  
Author(s):  
David T. Sullivan ◽  
L. Anne Bell ◽  
Duncan R. Paton ◽  
Marie C. Sullivan




1964 ◽  
Vol 39 (4) ◽  
pp. 240-253 ◽  
Author(s):  
SOTA HIRAGA


1985 ◽  
Vol 27 (1) ◽  
pp. 74-82
Author(s):  
J. A. Seawright ◽  
M. Q. Benedict ◽  
S. Narang

Snow (sn) is a recessive, eye color mutant that is phenotypically indistinguishable from the previously described mutant, white eye (we). The loci for these mutants are over 30 map units apart on the X chromosome. Analysis of salivary gland chromosomes of radiation-induced X-autosome translocations were used to define the positions of sn and we on the distal euchromatic portion of the long arm of the X chromosome. A recessive lethal trait (bubble head) was also mapped relative to we and sn, and the gene order on the long arm of the X chromosome is as follows: centromere – ? – snow – bubble head – white eye. Translocation breakpoints in the euchromatic portion of the X chromosome caused sterility or lethality in males hemizygous for the translocations, but breaks in the heterochromatin had no effect. Crossing-over was greatly reduced when translocation breakpoints were located in the euchromatic part of the X chromosome. The translocations were used to determine that the nucleolar organizer region is probably on the short arm of the X chromosome.Key words: Anopheles albimanus, eye colour mutant, X chromosome.



Genetics ◽  
1949 ◽  
Vol 34 (5) ◽  
pp. 564-572
Author(s):  
M M Green
Keyword(s):  


1964 ◽  
Vol 55 (5) ◽  
pp. 207-210 ◽  
Author(s):  
H. H. LAIDLAW ◽  
M. A. EL BANBY ◽  
K. W. TUCKER


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