Errata: A Quantitative Theory of Genetic Recombination and Chiasma Formation

Biometrics ◽  
1948 ◽  
Vol 4 (4) ◽  
pp. 246
Keyword(s):  
Genetic Recombination ◽  
Chiasma Formation ◽  
Quantitative Theory

scholarly journals Behaviour of Flanking Markers in Allelic Crosses

1966 ◽  
Vol 19 (6) ◽  
pp. 1047 ◽  
Author(s):  
DG Catcheside
Keyword(s):  
Fine Structure ◽  
Genetic Recombination ◽  
Genetic Differences ◽  
Quantitative Theory ◽  
Allelic Differences

The principles of analysis of the distributions of flanking markers amongst prototrophic recombinants arising from allelic auxotrophic differences are discussed. Considerable variations occur in the parameters which may be measured and also in the degree of agreement of criteria used to place allelic differences in order in fine structure maps. At least some of these variations appear likely to depend upon genetic differences affecting the mechanisms which result in genetic recombination and the mechanisms which control their activity. An approach to a quantitative theory of the distribution of flanking markers is suggested.

Electron Microscopy and image analysis of nucleo-protein complexes

1994 ◽  
Vol 52 ◽  
pp. 88-89
Author(s):  
E. H. Egelman ◽  
X. Yu
Keyword(s):  
Electron Microscopy ◽  
Image Analysis ◽  
Normal Cell ◽  
Genetic Recombination ◽  
Protein Complexes ◽  
Chromosomal Rearrangements ◽  
Reca Protein ◽  
E Coli ◽  
Helical Polymer ◽  
Specific Protease

The RecA protein of E. coli has been shown to mediate genetic recombination, regulate its own synthesis, control the expression of other genes, act as a specific protease, form a helical polymer and have an ATPase activity, among other observed properties. The unusual filament formed by the RecA protein on DNA has not previously been shown to exist outside of bacteria. Within this filament, the 36 Å pitch of B-form DNA is extended to about 95 Å, the pitch of the RecA helix. We have now establishedthat similar nucleo-protein complexes are formed by bacteriophage and yeast proteins, and availableevidence suggests that this structure is universal across all of biology, including humans. Thus, understanding the function of the RecA protein will reveal basic mechanisms, in existence inall organisms, that are at the foundation of general genetic recombination and repair.Recombination at this moment is assuming an importance far greater than just pure biology. The association between chromosomal rearrangements and neoplasms has become stronger and stronger, and these rearrangements are most likely products of the recombinatory apparatus of the normal cell. Further, damage to DNA appears to be a major cause of cancer.

A Quantitative Theory of War and Peace in the Gut Microbiota

2018 ◽  
Author(s):  
Libo Jiang ◽  
Xinjuan Liu ◽  
Mengmeng Sang ◽  
Jingwen Gan ◽  
Qian Wang ◽  
...  
Keyword(s):  
Gut Microbiota ◽  
War And Peace ◽  
Quantitative Theory ◽  
Theory Of War

Meiotic chromosome behavior of Haworthia limifolia

2016 ◽  
Vol 5 (03) ◽  
pp. 4902
Author(s):  
Afrin Nazli ◽  
Kamini Kumar*
Keyword(s):  
Genetic Recombination ◽  
Meiotic Chromosome ◽  
Pollen Sterility ◽  
Meiotic Abnormalities ◽  
Chromosome Behavior ◽  
The Family ◽  
Medicinal Properties ◽  
Fruit Formation ◽  
Meiosis I ◽  
Chromosomal Behaviour

Haworthia limifolia is a xerophytic plant belonging to the family Liliaceae and is indigenous to Africa. It is use extensively for its medicinal properties like antibacterial, antifungal properties and used for the treatment of sores, superficial burns, as a blood purifier and to promote pregnancy in women and cattles. In present investigation chromosomal behaviour of H. limifolia in meiosis was studied. In diplotene stage chiasmata was observed showing the possibilities of genetic recombination. Chromosome clumps were observed in diakinesis indicating sticky nature of chromosomes. Meiotic abnormalities like stickiness, precocious movement, formation of bridges and laggards were also reported in both meiosis I and II. A fairly high percentage of pollen sterility that is 73.41% was recorded resulting in failure of fruit formation. This plant could be designated as facultative apomict (Swanson, 1957) as the only means of reproduction found was asexual or vegetative.

Theileria parva ribosomal internal transcribed spacer sequences exhibit extensive polymorphism and mosaic evolution: application to the characterization of parasites from cattle and buffalo

Parasitology ◽  
1999 ◽  
Vol 118 (6) ◽  
pp. 541-551 ◽  
Author(s):  
N. E. COLLINS ◽  
B. A. ALLSOPP
Keyword(s):  
Genetic Recombination ◽  
Large Subunit ◽  
Small Subunit ◽  
Internal Transcribed Spacers ◽  
Rrna Genes ◽  
Gene Pools ◽  
Theileria Parva ◽  
Causative Agents ◽  
Internal Transcribed Spacer Sequences

We sequenced the rRNA genes and internal transcribed spacers (ITS) of several Theileria parva isolates in an attempt to distinguish between the causative agents of East coast fever and Corridor disease. The small subunit (SSU) and large subunit (LSU) rRNA genes from a cloned T. p. lawrencei parasite were sequenced; the former was identical to that of T. p. parva Muguga, and there were minor heterogeneities in the latter. The 5·8S gene sequences of 11 T. parva isolates were identical, but major differences were found in the ITS. Six characterization oligonucleotides were designed to hybridize within the variable ITS1 region; 93·5% of T. p. parva isolates examined were detected by probe TPP1 and 81·8% of T. p. lawrencei isolates were detected by TPL2 and/or TPL3a. There was no absolute distinction between T. p. parva and T. p. lawrencei and the former hybridized with fewer of the probes than did the latter. It therefore seems that a relatively homogenous subpopulation of T. parva has been selected in cattle from a more diverse gene pool in buffalo. The ITSs of both T. p. parva and T. p. lawrencei contained different combinations of identifiable sequence segments, resulting in a mosaic of segments in any one isolate, suggesting that the two populations undergo genetic recombination and that their gene pools are not completely separate.

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