recombination nodule
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2015 ◽  
Author(s):  
Cathleen M Lake ◽  
Rachel J Nielsen ◽  
Fengli Guo ◽  
Jay R Unruh ◽  
Brian D Slaughter ◽  
...  


Genome ◽  
1999 ◽  
Vol 42 (2) ◽  
pp. 308-314 ◽  
Author(s):  
M.I. Pigozzi ◽  
A.J. Solari


Genetics ◽  
1994 ◽  
Vol 137 (1) ◽  
pp. 281-288 ◽  
Author(s):  
M P Maguire ◽  
R W Riess

Abstract Frequency of homologous synapsis at pachytene for a relatively short heterozygous inversion was compared to the frequency of crossover occurrence within the inversion and to the frequency of the presence of a recombination nodule within the homologously synapsed inverted region. Crossover frequencies were estimated from bridge-fragment frequencies at anaphase I and anaphase II. Recombination nodules (RNs) were observed in electron micrographs. Results show very similar frequencies of homologous synapsis and the occurrence of reciprocal recombination within the inverted region, consistent with the interpretation that establishment of homologous synapsis in this case is related to at least commitment to the form of resolution of crossover intermediates which gives rise to reciprocal recombination, not conversion only, events. An RN was generally found at pachytene in homologously synapsed inverted regions.



BioEssays ◽  
1994 ◽  
Vol 16 (1) ◽  
pp. 69-74 ◽  
Author(s):  
Adelaide T. C. Carpenter
Keyword(s):  


Genome ◽  
1991 ◽  
Vol 34 (5) ◽  
pp. 718-726 ◽  
Author(s):  
Alberto J. Solari ◽  
M. H. Thorne ◽  
B. L. Sheldon ◽  
C. B. Gillies

Twelve triploid, ZZW chickens of ages ranging from day 19 of incubation to 15 days after hatching were used for oocyte analysis. Oocytes show 117 axes per nucleus. At early pachytene, most axes form double synaptonemal complexes (triplets). An average of 27 triplets, 12 bivalents, and 12 univalents was observed. Later, a partial elimination of triplets occurs, as they are converted into typical trivalents or bivalents and univalents. The number of recombination nodules per nucleus (52.7) is similar to that of diploids. These nodules can occur in register in both central regions of a triplet (no lateral interference), and they probably stabilize the central region. Among 31 oocytes, 29 had a regular ZZ bivalent and a W univalent, and only 2 had triple pairing between a ZZ bivalent and a terminal region of the W axis (less than 1 μm in length and having a terminal recombination nodule). Competition for pairing between the gonosomes results in a large (93.5% of cases) predominance of Z–Z pairing, because of a relatively minor homology between the W and Z chromosomes. The prevailing pairing failure of the W chromosome may lead to early oocyte loss.Key words: sex chromosomes, triploids, synaptonemal complex, Z–W pairing, chicken, recombination nodules.



Genome ◽  
1988 ◽  
Vol 30 (6) ◽  
pp. 900-902 ◽  
Author(s):  
A. J. Solari ◽  
N. S. Fechheimer

Synaptonemal complex analysis of an exceptional tetraploid oocyte from a diploid chicken heterozygous for the MN t (Z;1) rearrangement was performed by electron microscopy of a spread preparation. Ten separate quadrivalents (26% of the chromosomal axes) were analyzed, as well as 50 autosomal bivalents. All the axes less than 2.5 μm in length formed bivalents (38) only, while axes in the 2.5–4.2 μm range formed 5 quadrivalents and 12 bivalents. The longer, separate axes formed quadrivalents only. Partner switches in excess of one were documented. The two identical W chromosomes paired only at the ends of their short arms. Quadrivalent formation may require a threshold length (2.5 μm), at least in this species. The tip of the short arm of the W chromosome may be a pairing initiation point, and it corresponds to the region associated with a localized recombination nodule previously described in diploid oocytes.Key words: quadrivalent, tetraploid, synaptonemal complex, chicken oocyte.



1988 ◽  
Vol 48 (3) ◽  
pp. 130-136 ◽  
Author(s):  
A.J. Solari ◽  
N.S. Fechheimer ◽  
J.J. Bitgood
Keyword(s):  


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