Nonrandom segregation of the mouse univalent X chromosome: Evidence of spindle-mediated meiotic drive

Genetics

Volumn 156, Issue 2, 2000, Pages 775-783

  LeMaire Adkins, Renée ^a,b   Hunt, Patricia A ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CHROMOSOME SEGREGATION; CLINICAL FEATURE; CONFOCAL MICROSCOPY; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; IMMUNOFLUORESCENCE; MEIOSIS; MITOSIS SPINDLE; MOUSE; NONHUMAN; OOCYTE DEVELOPMENT; PREDICTION; PRIORITY JOURNAL; X CHROMOSOMAL INHERITANCE;

ANIMALS; CHROMOSOME DELETION; FEMALE; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MEIOSIS; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MITOTIC SPINDLE APPARATUS; OOCYTES; X CHROMOSOME;

EID: 0033790732     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (40)

1. Meiotic drive in female mice heterozygous for the HSR inserts on chromosome 1
2. Meiotic drive on aberrant chromosome 1 in the mouse is determined by a linked distorter
3. Effect of sperm genotype on chromatid segregation in female mice heterozygous for aberrant chromosome 1
4. The evolution of cooperation
5. Segregation distortion of X-linked marker genes in interspecific crosses between Mus musculus and M. spretus
6. X-chromosome segregation, maternal age and aneuploidy in the XO mouse
7. XO mice
8. Chromosomal drive and the evolution of meiotic nondisjunction and trisomy in humans
9. Translocation and amplification of an X-chromosome DNA repeat in inbred strains of mice
10. Assignment of genes to regions of mouse chromosomes
11. The mouse Y* chromosome involves a complex rearrangement, including interstitial positioning of the pseudoautosomal region
12. Yuichiro Hiraizumi and forty years of segregation distortion
13. Robertsonian translocations: Cytology, meiosis, segregation patterns and biological consequences of heterozygosity
14. Human aneuploidy: Incidence, origin, and etiology
15. Survival of XO mouse fetuses: Effect of parental origin of the X chromosome or uterine environment?
16. Analysis of chromosome behavior in intact mammalian oocytes: Monitoring the segregation of a univalent chromosome during female meiosis
17. B-chromosome drive
18. A generic linkage map of mouse chromosome 10: Localization of eighteen molecular markers using a single interspecific backcross
19. Non-random segregation during mammalian oogenesis
20. Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice
21. Lack of checkpoint control at the metaphase/anaphase transition: A mechanism of meiotic nondisjunction in mammalian females
22. Cytogenetic analysis of oocytes and early preimplantation embryos from XO mice
23. Epistatic control of non-Mendelian inheritance in mouse interspecific crosses
24. Susceptibility to vinblastine-induced aneuploidy and preferential chromosome segregation during meiosis I in Robertsonian heterozygous mice
25. Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome
26. A genetic test to determine the origin of maternal transmission ratio distortion: Meiotic drive at the mouse Om locus
27. The effect of abnormal chromosome 10 on preferential segregation and crossing over in maize
28. Chromarid cohesion during mitosis: Lessons from meiosis
29. Meiotic drive in female mice: An essay
30. The influence of mutations on chromosome 17 upon the segregation of homologues in female mice heterozygous for Robertsonian translocations
31. Increased incidence of unpartnered single chromatids in metaphase II oocytes in 39,X(XO) mice
32. Meiotic drive as an evolutionary force
33. The peculiar journey of a selfish chromosome: Mouse t haplotypes and meiotic drive
34. What determines whether chromosomes segregate reductionally or equationally in meiosis?
35. Interspecific backcross mice show sex-specific differences in allelic inheritance
36. Meiosis: Rec8 is the reason for cohesion
37. Two new X-autosome Robertsonian translocations in the mouse. I. Meiotic chromosome segregation in male hemlzygotes and female heterozygotes
38. A paternally imprinted X chromosome retards the development of the early mouse embryo
39. Cohesin Rec8 is required for reductional chromosome segregation at meiosis
40. Genetic variation in rates of nondisjunction: Association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster