Isolation and characterization of a retroelement from B chromosome (PSR) in the parasitic wasp Nasonia vitripennis

1995 ◽  
Vol 4 (4) ◽  
pp. 253-262 ◽  
Author(s):  
B. F. McAllister
Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 157-161 ◽  
Author(s):  
Kent M. Reed

Paternal sex ratio (PSR) is a B chromosome found in the parasitic wasp Nasonia vitripennis. PSR has a unique etiology in that it destroys the paternal chromosomes of fertilized eggs, resulting in the production of all male families. This study examined structural aspects of PSR including size, C-banding, and silver staining. PSR was found to constitute approximately 5.7% of the genome of carrier males. C-banding confirmed the heterochromatic nature of PSR and the data suggest that PSR remains primarily condensed throughout the cell cycle. Examination of prometaphase spermatocytes revealed a secondary constriction on PSR. The constriction, however, did not stain positive for nucleolus organizer activity. During mitosis, PSR and the pericentromeric regions of the A chromosomes displayed a temporal pattern of silver staining, involving dense precipitation of silver prior to metaphase. This reaction is indicative of a protein complex specific to the heterochromatin of these regions. The implications of these findings to the origin of PSR are discussed.Key words: Nasonia vitripennis, paternal sex ratio, B chromosome, nucleolus organizer region, heterochromatin.


Chromosoma ◽  
1997 ◽  
Vol 106 (4) ◽  
pp. 243-253 ◽  
Author(s):  
Bryant F. McAllister ◽  
John H. Werren

Genetics ◽  
1993 ◽  
Vol 133 (3) ◽  
pp. 637-648 ◽  
Author(s):  
L W Beukeboom ◽  
J H Werren

Abstract Paternal Sex Ratio (PSR) is a "selfish" B chromosome in the parasitoid wasp Nasonia vitripennis. It is transmitted via sperm, but causes supercondensation and destruction of the paternal chromosomes in early fertilized eggs. Because this wasp has haplodiploid sex determination, the effect of PSR is to convert diploid (female) eggs into haploid (male) eggs that carry PSR. Characterizing its genetic structure is a first step toward understanding mechanisms of PSR action. The chromosome is largely heterochromatic and contains several tandemly repeated DNA sequences that are not present on the autosomes. A deletion analysis of PSR was performed to investigate organization of repeats and location of functional domains causing paternal chromosome destruction. Deletion profiles using probes to PSR-specific repetitive DNA indicate that most repeats are organized in blocks on the chromosome. This study shows that the functional domains of PSR can be deleted, resulting in nonfunctional PSR chromosomes that are transmitted to daughters. A functional domain may be linked with the psr22 repeat, but function may also depend on abundance of PSR-specific repeats on the chromosome. It is hypothesized that the repeats act as a "sink" for a product required for proper paternal chromosome processing. Almost all deletion chromosomes remained either functional of nonfunctional in subsequent generations following their creation. One chromosome was exceptional in that it reverted from nonfunctionality to functionality in one lineage. Transmission rates of nonfunctional deletion chromosomes were high through haploid males, but low through diploid females.


2000 ◽  
Vol 31 (2) ◽  
pp. 149-149 ◽  
Author(s):  
T Tozaki ◽  
H Kakoi ◽  
S Mashima ◽  
K Hirota ◽  
T Hasegawa ◽  
...  

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
B Tóth ◽  
N Kúsz ◽  
A Csorba ◽  
T Kurtán ◽  
J Hohmann ◽  
...  

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