CYTOGENETICS OF A UNIVALENT CHROMOSOME IN BS DROSOPHILA MELANOGASTER MALES

1971 ◽  
Vol 13 (1) ◽  
pp. 81-89 ◽  
Author(s):  
R. C. Johnsen

Bs males bearing a modified X:4 translocation in which one of the members, XPYL∙YS, is an invariable univalent show that the univalent-bearing gametes from males raised at 26.0 °C are recovered only half as frequently as from those raised at 18.0 °C (Zimmering, 1963).Such males were raised at 26.0 °C (Experiments I and II) and at 18.0 °C (Experiment III) and upon eclosion were mated to three yellow free-X females for 3 days at 26.0 °C. Testes of sib males were squashed and examined with phase optics to follow the meiotic behavior of the univalent. All tests were carried out over a 3-year period.The genetic results confirm those of Zimmering (1963) and show that the univalent is recovered with a frequency of 22.5 ± 0.9% and 18.5 ± 0.9% in Experiments I and II, whereas it is recovered with a frequency of 36.7 ± 1.6% in Experiment III. However, the cytological results show that while the univalent lags at A I with a frequency of 9.4, 28.7, and 32.2%, respectively, cells with and without XPYL∙YS are observed with equal frequency at M II and A II in all experiments. The post meiotic stages also appear to be normal at the level of the light microscope. Although negligible loss of the univalent is not excluded, it is clear that the frequency of XPYL∙YS lag is unrelated to temperature or to the distorted genetic ratios from males raised at 26.0 °C. Degeneration of XPYL∙YS-bearing sperm beyond the level of the light microscope remains as a possible explanation for the observed genetic distortion.

2017 ◽  
Vol 216 (6) ◽  
pp. 1597-1608 ◽  
Author(s):  
Travis Karg ◽  
Mary Williard Elting ◽  
Hannah Vicars ◽  
Sophie Dumont ◽  
William Sullivan

Although poleward segregation of acentric chromosomes is well documented, the underlying mechanisms remain poorly understood. Here, we demonstrate that microtubules play a key role in poleward movement of acentric chromosome fragments generated in Drosophila melanogaster neuroblasts. Acentrics segregate with either telomeres leading or lagging in equal frequency and are preferentially associated with peripheral bundled microtubules. In addition, laser ablation studies demonstrate that segregating acentrics are mechanically associated with microtubules. Finally, we show that successful acentric segregation requires the chromokinesin Klp3a. Reduced Klp3a function results in disorganized interpolar microtubules and shortened spindles. Normally, acentric poleward segregation occurs at the periphery of the spindle in association with interpolar microtubules. In klp3a mutants, acentrics fail to localize and segregate along the peripheral interpolar microtubules and are abnormally positioned in the spindle interior. These studies demonstrate an unsuspected role for interpolar microtubules in driving acentric segregation.


Genetics ◽  
1975 ◽  
Vol 81 (2) ◽  
pp. 293-311
Author(s):  
David G Holm ◽  
Arthur Chovnick

ABSTRACT Studies of the meiotic distribution of compound-3 chromosomes in males and females of Drosophila melanogaster provided the following results. (1) From females homozygous for the standard arrangement of all chromosomes other than C(3L) and C(3R), less than 5% of the gametes recovered were nullosomic or disomic for compound-3 chromosomes. The frequency of nonsegregation differed between strains, but within a given strain it remained relatively constant. (2) According to egg-hatch frequencies, C(3L) and C(3R) segregate independently during spermatogenesis. (3) In females, structurally heterozygous second chromosomes occasion a marked increase in the recovery of nonsegregational progeny; in males, rearranged seconds have no apparent influence on the distribution of compound thirds. (4) The highest frequencies of nonsegregational progeny were recovered from C(3L);C(3R) females carrying compound-X (plus free Y) chromosomes. (5) In comparing the recovery of nonsegregating compound thirds to the recovery of rearranged heterologs, a definite nonrandom distribution was realized in several crosses. These results are examined in reference to the concepts of distributive pairing (Grell 1962). Moreover, considering the structural nature of compound autosomes, we propose that nonhomologous (distributive) pairing is a property of the centromeric region and suggest that rearrangements involving breaks in this region possibly alter the effectiveness of distributive pairing forces.


1978 ◽  
Vol 31 (3) ◽  
pp. 303 ◽  
Author(s):  
JA Sved

Recombinant second chromosomes from dysgenic male hybrids of D. melanogaster have been made homozygous using a Curly balancer chromosome technique. Most of the chromosome homozygotes produced have apparently normal viability. The incidence of newly produced lethals, while as high as 5-10%, is not significantly higher than in non-recombinant chromosomes. Thus male recombination and mutation appear to occur independently of each other, rather than in the same gametes as would be expected if both were simultaneously produced by chromosome breakage and reunion. Furthermore, a summary of recombination clusters over a large series of experiments suggests that reciprocal and non-reciprocal clusters occur with approximately equal frequency. This is in agreement with predictions from a four-strand mitotic recombination model.


Genetics ◽  
1973 ◽  
Vol 73 (4) ◽  
pp. 631-638
Author(s):  
S Zimmering ◽  
E B Bendbow

ABSTRACT Crossing over in the interstitial region of the heterozygous V4 translocation in Drosophila melanogaster generates asymmetric dyads each consisting of a shorter and a longer chromatid It was shown previously that in the female the shorter is recovered preferentially (ZIMMERING 1955); the present work suggests that the same occurs in the male as weI1. The mechanism in the female is envisioned as involving the non-random inclusion of the shorter chromatid into the functional egg (NOVITSK 1951); in the male, the two formal possibilities appear to be (1) that some proportion of sperm carrying the longer chromatid derived from an asymmetric dyad undergoes dysfunction, or (2) the longer chromatid is preferentially included into regularly-produced nonfunctional sperm, the nonfunctionality set up at the second division and distinguishing second division daughter cells.


1985 ◽  
Vol 38 (1) ◽  
pp. 1 ◽  
Author(s):  
Ronald J Hill

A method has been developed which, for the first time, allows the preparation of mappable cytological spreads of salivary chromosomes from D. melanogaster without exposure to acid fixatives. These isolated native chromosomes show the best preservation of ultrastructure observed to date-ribonucleoprotein particles may be seen to be organized in linear arrays in transcriptionally active puffs and the repeating nucleosome module is present. Native salivary chromosomes are proving useful for the localization of nuclear proteins both at the light microscope and ultrastructural levels. They display only background-level binding of antibodies specific for the Z-DNA conformation. However, Z-DNA immunoreactivity is activated by exposure to acid fixative, first in interbands and then in bands. The Z-conformation in the chromosomes is held in place by elastic torsional strain which appears in the DNA following acid fixation. Native D. melanogaster salivary chromosomes offer promise for enabling the probing of the chromatin of known genetic loci for properties dependent on the preservation of macromolecular integrity.


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