scholarly journals MODIFICATION OF RECOMBINATION FREQUENCY IN DROSOPHILA. I. SELECTION FOR INCREASED AND DECREASED CROSSING OVER

Genetics ◽  
1971 ◽  
Vol 69 (1) ◽  
pp. 71-83
Author(s):  
Joseph P Chinnici
1984 ◽  
Vol 44 (2) ◽  
pp. 199-217 ◽  
Author(s):  
Alexey S. Kondrashov

SUMMARYA population with u deleterious mutations per genome per generation is considered in which only those individuals that carry less than a critical number of k mutations are viable. It has been shown previously that under such conditions sexual reproduction is advantageous. Here we consider selection at a locus that determines recombination frequency of the whole genome. The value v = u/ √ k has been found to play the decisive role. When v < 0·35 the direction of selection for recombination may be different for different cases, but the intensity of selection is always very small. The advantage of recombination becomes considerable when v > 0·5, its growth under increasing v being approximately linear. If v > 2 no less than 95% of the progeny are bound to die because of the selection against deleterious mutations. Since this seems to be too great a mutation load, we may assume 0·5 < v < 2·0 for any sexual population if mutation really maintains crossing-over. Results on selection at a locus which controls mutability provide evidence that v is located within the specified interval if the physiological cost of a twofold reduction of the mutation rate is within the range 10–80%. A number of consequences of this hypothesis about the mechanism of selection for sex and recombination are discussed.


1970 ◽  
Vol 6 (3) ◽  
pp. 669-678
Author(s):  
B. C. LU

The frequency of genetic recombination in Coprinus lagopus may be modified by heat and cold shock. By removal of samples from a fruiting body before and after temperature treatment, it is possible to study the ultrastructure of chromosomes at the time recombination frequency (between den+ x +me-1) can be modified. The sensitive period for temperature effects and, therefore, probably the time of crossing over, commences with the formation of the synaptinemal complex (S.C.) and ends with its disappearance, i.e. during the entire existence of the S.C. It is concluded that recombination is an event subsequent to the formation of the S.C. and is independent of the process of its formation. It is suggested that the event takes place at the synaptic centre.


1975 ◽  
Vol 26 (2) ◽  
pp. 203-211 ◽  
Author(s):  
Graig Hammerberg ◽  
Jan Klein

SUMMARYLinkage data for the following markers on chromosome 17 of the house mouse were obtained: centromere (marked by translocation R67), Brachyury (T), tufted (tf), H-2, and thin fur (thf). The markers were found to be arranged in that order in the genetic map and the combined genetic distances between individual markers were found to be as follows: Rb7…T, 4·5 cM; T…tf, 5·8 cM; tf…H-2, 5·0 cM; H-2…thf, 15·1 cM. The localization of the thf locus on the non-centromeric side of the H-2 complex provides an important marker for this arm of chromosome 17. The map distances in the centromeric portion of chromosome 17 changed drastically in the presence of various t factors. These factors strongly reduce the recombination frequency in the T…tf and tf…H-2 intervals and this crossing-over suppression is most likely responsible for the linkage disequilibrium between t and H-2 reported earlier. Recombinants involving a t chromosome but occurring to the right of the H-2 complex do not change the properties of t factors suggesting that all determinants responsible for the t phenotype are located in the chromosomal region between T and tf (H-2).


Genome ◽  
1999 ◽  
Vol 42 (2) ◽  
pp. 248-253 ◽  
Author(s):  
Takao Komatsuda ◽  
Wenbin Li ◽  
Fumio Takaiwa ◽  
Seibi Oka

The vrs1 (formerly v) locus in the long arm of chromosome 2H controls lateral spikelet development in barley. The vrs1 locus was mapped by backcross-derived lines that consisted of 373 BC7F1 plants and 278 BC6F2 plants. The linkage study indicated that MWG801, CMNA-38/700, cMWG699, vrs1 and MWG865 exist in the order listed, with map distances of 3.1, 0.4, 0.1, and 0.9 centimorgans (cM), respectively. Recombination in female and male meiocytes showed no significant difference within this region. In a neighboring region between MWG865 and MWG503, the recombination frequency was higher in female than male meiocytes in one mapping population. The combined linkage data obtained from this study were compared with published data, and genotype-specific suppression of crossing-over was not evident in the vrs1 region.Key words: vrs1 locus (two- vs. six-rowed), molecular marker, recombination, backcross, Hordeum vulgare.


2020 ◽  
Author(s):  
Fadi G. Alnaji ◽  
Kirsten Bentley ◽  
Ashley Pearson ◽  
Andrew Woodman ◽  
Jonathan D. Moore ◽  
...  

ABSTRACTRecombination within RNA viruses is an important evolutionary process that can significantly influence virus fitness and has been repeatedly reported to compromise vaccine effectiveness. However, its precise mechanism is poorly understood. Here, we used an established poliovirus-based in vitro assay (CRE-REP) to investigate the molecular determinants of recombination and show that neither sequence identity, nor RNA structure, have any significant effect on recombination frequency. Since the CRE-REP assay is confined by the ability to detect infectious virus progeny, we utilized deep sequencing to study the recombinant genome population that arises early in infection and before any bottleneck of selection for viable progeny. We were able to detect and analyse hundreds of recombinants containing sequence insertions or deletions, or that were of wild type genome length. While we found higher diversity in recombination events than from CRE-REP assays, the analyses demonstrate no biases towards sequence or structure, in support of the CRE-REP assay findings. The results suggest that genome functionality and fitness are of greater importance in determining the identity of recombinants. These studies provide critical information that can improve our understanding of the recombination process, and consequently allow for the production of less recombinogenic and more stable vaccines.


2020 ◽  
Vol 10 (6) ◽  
pp. 2103-2110
Author(s):  
Ramswaroop Saini ◽  
Amit Kumar Singh ◽  
Geoffrey J. Hyde ◽  
Ramamurthy Baskar

Crossing over, the exchange of DNA between the chromosomes during meiosis, contributes significantly to genetic variation. The rate of crossovers (CO) varies depending upon the taxon, population, age, external conditions, and also, sometimes, between the sexes, a phenomenon called heterochiasmy. In the model plant Arabidopsis thaliana, the male rate of all crossover events (mCO) is typically nearly double the female rate (fCO). A previous, PCR-based genotyping study has reported that the disparity decreases with increasing parental age, because fCO rises while mCO remains stable. We revisited this topic using a fluorescent tagged lines approach to examine how heterochiasmy responded to parental age in eight genomic intervals distributed across the organism’s five chromosomes. We determined recombination frequency for, on average, more than 2000 seeds, for each interval, for each of four age groups, to estimate sex-specific CO rates. mCO did not change with age, as reported previously, but, here, fCO did not rise, and thus the levels of heterochiasmy were unchanged. We can see no methodological reason to doubt that our results reflect the underlying biology of the accessions we studied. The lack of response to age could perhaps be due to previously reported variation in CO rate among accessions of Arabidopsis.


1988 ◽  
Vol 51 (2) ◽  
pp. 89-93 ◽  
Author(s):  
B. Rattray ◽  
A. M. Rose

SummaryThe Rec-1 strain of Caenorhabditis elegans increases recombination frequency three-fold. In this paper, we have investigated the effect of Rec-1 on the intragenic recombination phenomena of crossing-over and gene conversion. These events were increased two- to three-fold as was X-chromosome non-disjunction. All of the recovered recombinants were independent events, indicating that Rec-1 does not act pre-meiotically. The pattern of recombination in the Rec-1 strain resembles a meiotic pattern more than a radiation expansion. We conclude from this result that the Rec-1 enhancement of recombination is not the result of an increased number of DNA lesions randomly distributed along the chromosome. The increased recombination frequency of Rec-1 was not accompanied by any detrimental effects on growth, progeny number or spontaneous mutation rate. In this regard, the results may have implications for models which propose either selective advantage or disadvantage accompanying increased recombination.


Genetica ◽  
1985 ◽  
Vol 67 (1) ◽  
pp. 73-78 ◽  
Author(s):  
A. A. Zhuchenko ◽  
A. B. Korol ◽  
L. P. Kovtyukh

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