PULSED-FIELD MAP OF XQ13 IN THE REGION OF THE HUMAN-X INACTIVATION CENTER

被引:14
作者
LAFRENIERE, RG
WILLARD, HF
机构
[1] CASE WESTERN RESERVE UNIV,SCH MED,DEPT GENET,10900 EUCLID AVE,CLEVELAND,OH 44106
[2] CASE WESTERN RESERVE UNIV,SCH MED,CTR HUMAN GENET,CLEVELAND,OH 44106
关键词
D O I
10.1006/geno.1993.1356
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have used human/mouse hybrid cell lines to derive a pulsed-field map of the Xq13 region of the human X chromosome, in the vicinity of the X inactivation center (XIC). We have mapped nine loci within two separate clusters (I and II). Cluster I contains three loci (DXS227, XIST, and DXS128) linked within 1700 kb. This cluster also includes the breakpoint of a translocated X;14 chromosome used to define the proximal border of the XIC region. Cluster II covers an additional 1800 kb and physically links six loci (DXS56, DXS171, DXS325, DXS347, DXS356, and DXS441) located between the XIC and the genes for Menkes disease (MNK) and PGK1. Maps of cluster I loci derived from active (Xa) or inactive (Xi) X chromosomes differed, presumably due to methylation differences between the Xa and Xi. This map provides a basis for examining the organization of the Xq13.2-q13.3 region, in and around the XIC, and will assist in the further cloning of expressed sequences from this region. © 1993 by Academic Press, Inc.
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页码:502 / 506
页数:5
相关论文
共 13 条
[1]  
BERGOFFEN J, 1993, AM J HUM GENET, V52, P312
[2]   GENE ON SHORT ARM OF HUMAN-X CHROMOSOME COMPLEMENTS MURINE TSA1S9 DNA-SYNTHESIS MUTATION [J].
BROWN, CJ ;
POWERS, VE ;
MUNROE, DL ;
SHEININ, R ;
WILLARD, HF .
SOMATIC CELL AND MOLECULAR GENETICS, 1989, 15 (02) :173-178
[3]   LOCALIZATION OF THE X-INACTIVATION CENTER ON THE HUMAN X-CHROMOSOME IN XQ13 [J].
BROWN, CJ ;
LAFRENIERE, RG ;
POWERS, VE ;
SEBASTIO, G ;
BALLABIO, A ;
PETTIGREW, AL ;
LEDBETTER, DH ;
LEVY, E ;
CRAIG, IW ;
WILLARD, HF .
NATURE, 1991, 349 (6304) :82-84
[4]  
BROWN CJ, 1989, AM J HUM GENET, V45, P592
[5]   FINE MAPPING AND CLONING OF THE BREAKPOINT ASSOCIATED WITH MENKES SYNDROME IN A FEMALE-PATIENT [J].
CONSALEZ, GG ;
GECZ, J ;
STAYTON, CL ;
DABOVIC, B ;
PASINI, B ;
PEZZOLO, A ;
BICOCCHI, MP ;
FONTES, M ;
ROMEO, G .
GENOMICS, 1992, 14 (03) :557-561
[6]   26 PATIENTS WITH HEMATOLOGIC DISORDERS AND X-CHROMOSOME ABNORMALITIES FREQUENT IDIC(X)(Q13) CHROMOSOMES AND XQ13 ANOMALIES ASSOCIATED WITH PATHOLOGIC RINGED SIDEROBLASTS [J].
DEWALD, GW ;
BRECHER, M ;
TRAVIS, LB ;
STUPCA, PJ .
CANCER GENETICS AND CYTOGENETICS, 1989, 42 (02) :173-185
[7]   DELINEATION OF THE DYSTONIA PARKINSONISM SYNDROME LOCUS IN XQ13 [J].
GRAEBER, MB ;
KUPKE, KG ;
MULLER, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8245-8248
[8]   PHYSICAL MAPPING OF 60DNA MARKERS IN THE P21.1-]Q21.3 REGION OF THE HUMAN X-CHROMOSOME [J].
LAFRENIERE, RG ;
BROWN, CJ ;
POWERS, VE ;
CARREL, L ;
DAVIES, KE ;
BARKER, DF ;
WILLARD, HF .
GENOMICS, 1991, 11 (02) :352-363
[9]   STRUCTURAL ANOMALIES OF THE X-CHROMOSOME AND INACTIVATION CENTER [J].
MATTEI, MG ;
MATTEI, JF ;
VIDAL, I ;
GIRAUD, F .
HUMAN GENETICS, 1981, 56 (03) :401-408
[10]  
RASKIND WH, 1991, AM J HUM GENET, V48, P335