Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci

Genomics ◽  
1989 ◽  
Vol 5 (2) ◽  
pp. 382-384 ◽  
Author(s):  
R WOLFF
Genetics ◽  
1990 ◽  
Vol 126 (1) ◽  
pp. 261-276
Author(s):  
T Nagylaki

Abstract The evolution of the probabilities of genetic identity within and between the loci of a multigene family dispersed among multiple chromosomes is investigated. Unbiased gene conversion, equal crossing over, random genetic drift, and mutation to new alleles are incorporated. Generations are discrete and nonoverlapping; the diploid, monoecious population mates at random. The linkage map is arbitrary, but the same for every chromosome; the dependence of the probabilities of identity on the location on each chromosome is formulated exactly. The greatest of the rates of gene conversion, random drift, and mutation is epsilon much less than 1. Under the assumption of loose linkage (i.e., all the crossover rates greatly exceed epsilon, though they may still be much less than 1/2), explicit approximations are obtained for the equilibrium values of the probabilities of identity and of the linkage of disequilibria. The probabilities of identity are of order one [i.e., O(1)] and do not depend on location; the linkage disequilibria are of O(epsilon) and, within each chromosome, depend on location through the crossover rates. It is demonstrated also that the ultimate rate and pattern of convergence to equilibrium are close to that of a much simpler, location-independent model. If intrachromosomal conversion is absent, the above results hold even without the assumption of loose linkage. In all cases, the relative errors are of O(epsilon). Even if the conversion rate between genes on nonhomologous chromosomes is considerably less than between genes on the same chromosome or homologous chromosomes, the probabilities of identity between the former genes are still almost as high as those between the latter, and the rate of convergence is still not much less than with equal conversion rates. If the crossover rates are much less than 1/2, then most of the linkage disequilibrium is due to intrachromosomal conversion. If linkage is loose, the reduction of the linkage disequilibria to O(epsilon) requires only O(-ln epsilon) generations.


Author(s):  
Masreshaw Yirga

Polyploidy is a prominent force of shaping the evolution of in most of ferns and flowering plants. Polyploidy has tremendous contribution in plants improvement program. It is the polyploidy breeding through which new crops can be developed and interspecific genes can be transferred and also the origin of crops can be traced. It is now an interesting field of study to reveal the evolution of crop plants and utilizing their variability in the field of crop breeding. Polyploidy generally differ markedly from their progenitors in morphological, ecological, physiological and cytological characteristics that can contribute both to exploitation of a new niche and to reproductive isolation. As a result, polyploidy is a major mechanism of adaptation and speciation in plants. Another implication of polyploidy is development heterosis in plant breeding. Unlike diploids which may lose heterosis with each consecutive generation due to segregation, polyploidy imposes pairing of homologous chromosomes, thus preventing intergenomic recombination. In this way, heterozygosity is maintained throughout generations. One of the immediate and obvious consequences of polyploidy in plants is an increase in cell size which in turn leads to enlarged plant organs relative to diploids. It is also used in bridge crossing, development of seedless fruits like watermelon and production of apomictic crops.


Author(s):  
T. Guha ◽  
A. Q. Siddiqui ◽  
P. F. Prentis

The Primary Spermatocytes represent a stage in spermatogenesis when the first meiotic cell division occurs. They are derived from Spermatogonium or Stem cell through mitotic division. At the zygotene phase of meiotic prophase the Synaptonemal complex appears in these cells in the space between the paired homologous chromosomes. Spermatogenesis and sperm structure in fish have been studied at the electron microscope level in a few species? However, no work has yet been reported on ultrastructure of tilapia, O. niloticus, spermatozoa and spermatogenetic process. In this short communication we are reporting the Ultrastructure of Primary Spermatocytes in tilapia, O. niloticus, and the fine structure of synaptonemal complexes seen in the spermatocyte nuclei.


2006 ◽  
Vol 34 (2-3) ◽  
pp. 941-948 ◽  
Author(s):  
Tomislav Zivanovic ◽  
Savo Vuckovic ◽  
Slaven Prodanovic ◽  
Goran Todorovic

2011 ◽  
Vol 33 (2) ◽  
pp. 163-167 ◽  
Author(s):  
Zhang-Yuan PAN ◽  
Lan YE ◽  
Jing ZHU ◽  
Zi-Dong DU ◽  
Xiao-Guo HUANG ◽  
...  
Keyword(s):  
I Gene ◽  

Crop Science ◽  
1984 ◽  
Vol 24 (5) ◽  
pp. 945-947
Author(s):  
Joshua A. Lee
Keyword(s):  

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