MOLECULAR CYTOGENETIC CHARACTERIZATION OF 2 TYPES OF CHROMOSOME-9 VARIANTS

被引:13
|
作者
WANG, JCC [1 ]
MILLER, WA [1 ]
机构
[1] PRENATAL DIAGNOST CTR,LEXINGTON,MA
来源
CYTOGENETICS AND CELL GENETICS | 1994年 / 67卷 / 03期
关键词
D O I
10.1159/000133820
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Structural variations in the pericentromeric region of chromosome 9 are common. Molecular cytogenetic characterization of two types of rare variants, each studied in two families, are reported. For convenience, the variants are designated as types 2 and 3. Type 2 variants contain an additional G-positive band in the short arm near the centromere. Type 3 variants have heterochromatin both above and below the centromere in addition to having an additional G-positive band in the short arm immediately distal to the heterochromatin. Fluorescence in situ hybridization using alpha-satellite and D9Z5 beta-satellite probes revealed two clear hybridization signals in type 3 variants, one corresponding to the position of the centromere and the other to the position of the additional G-positive band. Results of type 2 variants are less conclusive, probably due to the close proximity of the additional band to the centromere, but are suggestive of additional hybridization in proximal 9p. Our finding suggests that the type 3 variant, and possibly the type 2 variant, may represent dicentric chromosomes that are functionally stable and phenotypically inconsequential.
引用
收藏
页码:190 / 192
页数:3
相关论文
共 50 条
  • [21] RARE VARIANT OF CHROMOSOME-9
    DOCHERTY, Z
    HULTEN, MA
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (01): : 105 - 106
  • [22] PERICENTRIC-INVERSION OF CHROMOSOME-9 AND A REARRANGEMENT INVOLVING CHROMOSOME-9 AND CHROMOSOME-10, OBSERVED IN 2 GENERATIONS - CLINICAL DESCRIPTION OF CHROMOSOME-9 (P12-P21) DELETION SYNDROME
    FALLSTROM, SP
    WAHLSTROM, J
    CLINICAL GENETICS, 1979, 15 (06) : 480 - 486
  • [23] CONSTRUCTION AND CHARACTERIZATION OF RADIATION HYBRIDS FOR CHROMOSOME-9, AND THEIR USE IN MAPPING COSMID PROBES ON THE CHROMOSOME
    JACKSON, CL
    BRITT, DE
    GRAW, SL
    POTTS, A
    SANTORO, K
    BUCKLER, AJ
    HOUSMAN, DE
    MARK, HFL
    SOMATIC CELL AND MOLECULAR GENETICS, 1992, 18 (03) : 285 - 301
  • [24] MOLECULAR ANALYSIS OF DELETIONS OF THE SHORT ARM OF CHROMOSOME-9 IN HUMAN GLIOMAS
    OLOPADE, OI
    JENKINS, RB
    RANSOM, DT
    MALIK, K
    POMYKALA, H
    NOBORI, T
    COWAN, JM
    ROWLEY, JD
    DIAZ, MO
    CANCER RESEARCH, 1992, 52 (09) : 2523 - 2529
  • [25] N-RAS-LIKE SEQUENCES ON CHROMOSOME-9, CHROMOSOME-6 AND CHROMOSOME-22 WITH A POLYMORPHISM AT THE CHROMOSOME-9 LOCUS
    MIDDLETONPRICE, H
    SPURR, N
    HALL, A
    MALCOLM, S
    ANNALS OF HUMAN GENETICS, 1988, 52 : 189 - 195
  • [26] POLYMORPHISM OF CHROMOSOME-9 AND HEMATOLOGIC DISORDERS
    CHEN, Z
    MORGAN, R
    STONE, JF
    SANDBERG, AA
    BLOOD, 1994, 84 (10) : A630 - A630
  • [27] INTEGRATION OF GENE MAPS FOR CHROMOSOME-9
    COLLINS, A
    LAWRENCE, S
    SHIELDS, DC
    MORTON, NE
    CYTOGENETICS AND CELL GENETICS, 1993, 64 (02): : 110 - 110
  • [28] ISOCHROMOSOME-FORMATION IN CHROMOSOME-9
    MILLER, K
    ARSLANKIRCHNER, M
    ANNALES DE GENETIQUE, 1994, 37 (02): : 78 - 81
  • [29] CHROMOSOME-9 IN VARIANT PH TRANSLOCATIONS
    ISHIHARA, T
    MINAMIHISAMATSU, M
    TOSUJI, H
    CANCER GENETICS AND CYTOGENETICS, 1985, 14 (1-2) : 183 - 184
  • [30] AN INDEX MARKER MAP OF CHROMOSOME-9
    KWIATKOWSKI, DJ
    DIB, C
    SLAUGENHAUPT, S
    POVEY, S
    GUSELLA, JF
    HAINES, JL
    CYTOGENETICS AND CELL GENETICS, 1993, 64 (02): : 115 - 115