메뉴 건너뛰기




Volumn 273, Issue 5271, 1996, Pages 118-122

Centric heterochromatin and the efficiency of achiasmate disjunction in Drosophila female meiosis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME CHIASM; DROSOPHILA; FEMALE; HETEROCHROMATIN; MEIOSIS; MITOSIS SPINDLE; NONDISJUNCTION; NONHUMAN; PRIORITY JOURNAL;

EID: 0030016870     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.273.5271.118     Document Type: Article
Times cited : (173)

References (64)
  • 4
    • 0002821334 scopus 로고
    • M. Ashburner and E, Novitski, Eds. (Academic Press, London)
    • R. F. Grell, in The Genetics and Biology of Drosophila, M. Ashburner and E, Novitski, Eds. (Academic Press, London, 1976), vol. 1a. pp. 435-486.
    • (1976) The Genetics and Biology of Drosophila , vol.1 A , pp. 435-486
    • Grell, R.F.1
  • 9
    • 0026658653 scopus 로고
    • _, Genetics 132, 737 (1992).
    • (1992) Genetics , vol.132 , pp. 737
  • 12
    • 9344261938 scopus 로고    scopus 로고
    • data not shown
    • G. H. Karpen, data not shown.
    • Karpen, G.H.1
  • 13
    • 9344221816 scopus 로고    scopus 로고
    • note
    • Random disjunction of these minichromosomes in males iS most likely explained by the fact that Dp1187, which is derived from the X chromosome (8), does not contain the normal X-Y pairing site (ribosomal DNA) (46, 47).
  • 14
    • 9344270666 scopus 로고    scopus 로고
    • note
    • Drosophilla females use an achiasmate disjunction system to disjoin Dp1187 homologs. First, the minichromosome is derived from two regions that normally exhibit very few reciprocal exchanges (the X tip and the X centric heterochromatin) (31), and as expected there is no observed recombination between Dp1187 homologs (48). Second, Dp1187 transmission and segregation are altered (18, 49) in animals that contain mutations that predominantly affect achiasmate chromosomes [for example. nod and ncd (50, 51)]. Third, Dp1187 homologs are positioned between the metaphase plate and the poles (52), a cytological characteristic of achiasmate chromosomes (53).
  • 15
    • 9344245878 scopus 로고    scopus 로고
    • note
    • Note that the greater disjunction of γ238/γ238 and γ158/γ158 (1 and 2% ND, respectively; Fig. 1B) in comparison to that for γ158 /Dp1187 and γ238/Dp1187 (5 and 6% ND, respectively; Fig. 1A) makes the lack of improvement seen for 10B/10B and γ1230/γ1230 even more significant.
  • 16
    • 9344269566 scopus 로고    scopus 로고
    • note
    • The +150 to +580 disjunction element is defined by the difference between the γ840 (normal disjunction) and γ1230 (abnormal disjunction) break-points. The +580 to +1000 region must contain significant disjunction function, because the observed 11% nondisjunction of γ1230 from Dpi1187 is substantially less than the 50% expected for random disjunction.
  • 21
    • 9344271687 scopus 로고    scopus 로고
    • note
    • For example, 30A/31E females (Fig. 2A) produced 8.7% y- ry+ progeny (0 Dp nondisjunction class) and 8.2% y+ ry+ progeny (2 Dp nondisjunction class); these values are not statistically different (two-tailedt test assuming unequal variances, t = 0.73). Similar results were obtained with other combinations of stably transmitted but aberrantly disjoining chromosomes.
  • 23
    • 0018484514 scopus 로고
    • _, Genetics 92, 511 (1979).
    • (1979) Genetics , vol.92 , pp. 511
  • 39
    • 0029937208 scopus 로고    scopus 로고
    • A. K. Csink and S. Henikoff Nature 381, 529 (1996); A. F. Dernburg et al., Cell 85, 745 (1996).
    • (1996) Nature , vol.381 , pp. 529
    • Csink, A.K.1    Henikoff, S.2
  • 40
    • 0029943141 scopus 로고    scopus 로고
    • A. K. Csink and S. Henikoff Nature 381, 529 (1996); A. F. Dernburg et al., Cell 85, 745 (1996).
    • (1996) Cell , vol.85 , pp. 745
    • Dernburg, A.F.1
  • 50
    • 9344244890 scopus 로고    scopus 로고
    • unpublished data
    • G. H. Karpen, unpublished data.
    • Karpen, G.H.1
  • 58
    • 9344239517 scopus 로고    scopus 로고
    • note
    • + genes observed in some Dpi 187 derivatives (10, 11, 18). This cross produces both X/X∧Y and X/O progeny, but X/O males were not scored, because of their enhanced variegation.
  • 59
    • 9344226931 scopus 로고    scopus 로고
    • note
    • The true nondisjunction rate (TND) corrected for chromosome loss was calculated for each female with the formula 50% X [frequency y+ ry+/(frequency y+ X frequency ry+)], as described previously (18). The numerator in the TND calculation is the observed frequency of progeny receiving both minichromosomes (unequivocal nondisjunction events, 2 Dp class; Fig. 1B); the denominator is the frequency of both minichromosomes segregating independently. This ratio will equal 1 if disjunction occurs at random; it is multiplied by 50% to specify random disjunction as 50%. It is important to note that the TND is identical to the standard ND frequency [100% X (exceptions/total)] for all cases except disjunction tests involving the partially unstable chromosomes J21A, 25A, and 1B; all data are presented as TND merely for consistency. The overall frequencies of y+ or ry+ progeny reflect the transmission rates of each minichromosome. All transmission and nondisjunction frequencies were measured in at least two independent experiments and reproduced to within 5% in all cases. Between 11 and 46 individual females were crossed in each experiment, and an average of 92 progeny per female were scored. Statistical tests (t tests) were performed as described (11, 18); only differences associated with P values less than 0.05 were considered significant.
  • 60
    • 9344242552 scopus 로고    scopus 로고
    • note
    • +) P element insertions at -246 and -185 (9, 55). 31E, 20A, 3B, 30A, 10B, 1B, 25A, and J21A are terminal deletion derivatives of the γ238 inversion (11).
  • 62
    • 9344221815 scopus 로고    scopus 로고
    • note
    • 1 parents and the appropriateness of using the 0 Dp class to estimate nondisjunction.
  • 63
    • 9344220092 scopus 로고    scopus 로고
    • note
    • +)/Sp ; ry males. All test females were crossed and the results analyzed as described (56, 57).
  • 64
    • 9344257455 scopus 로고    scopus 로고
    • note
    • + -15), J. Simon for the artwork in Fig. 4, and A. Dernburg, J. Sedat, and S. Hawley for communicating results before publication. This research was supported by a grant from the American Cancer Society (DB-1200), which we gratefully acknowledge.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.