A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1)

被引:22
作者
Kioschis, P
Rogner, UC
Pick, E
Klauck, SM
Heiss, N
Siebenhaar, R
Korn, B
Coy, JF
Laporte, J
LiechtiGallati, S
Poustka, A
机构
[1] DEUTSCH KREBSFORSCHUNGSZENTRUM,ABT MOL GENOMANAL,D-69120 HEIDELBERG,GERMANY
[2] C U STRASBOURG,INSERM U184,CNRS,GENET MOLEC EUCARYOTES LAB,ILLKIRCH GRAFFENS,FRANCE
[3] INST KLIN PHARMAKOL,CH-3008 BERN,SWITZERLAND
关键词
D O I
10.1006/geno.1996.0212
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
The X-linked myotubular myopathy locus (MTM1) has been assigned to the Xq28 region by linkage analysis. By observation of an interstitial deletion in a female patient, the candidate region could be further reduced to a region of 600 kb flanked by the markers DXS304 and DXS497. We describe here cosmid contigs covering a region of 900 kb, including the entire MTM1 candidate region. Cosmids from the region were used to construct an enriched cDNA library from this area. Filter grids carrying this library were then screened by hybridization with whole cosmid clones, with CpG island-containing fragments from linking clones located in the area, and with total exon trap products of cosmid clones from the candidate region. In this analysis, 10 new transcripts were identified and localized precisely within the map. Genes in this area are candidates for MTM1 and a number of other diseases localized by genetic linkage studies to the chromosomal band Xq28. (C) 1996 Academic Press, Inc.
引用
收藏
页码:365 / 373
页数:9
相关论文
共 61 条
  • [1] RAPID CDNA SEQUENCING (EXPRESSED SEQUENCE TAGS) FROM A DIRECTIONALLY CLONED HUMAN INFANT BRAIN CDNA LIBRARY
    ADAMS, MD
    SOARES, MB
    KERLAVAGE, AR
    FIELDS, C
    VENTER, JC
    [J]. NATURE GENETICS, 1993, 4 (04) : 373 - 386
  • [2] SEQUENCE IDENTIFICATION OF 2,375 HUMAN BRAIN GENES
    ADAMS, MD
    DUBNICK, M
    KERLAVAGE, AR
    MORENO, R
    KELLEY, JM
    UTTERBACK, TR
    NAGLE, JW
    FIELDS, C
    VENTER, JC
    [J]. NATURE, 1992, 355 (6361) : 632 - 634
  • [3] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [4] DYSKERATOSIS-CONGENITA - 3 ADDITIONAL FAMILIES SHOW LINKAGE TO A LOCUS IN XQ28
    ARNGRIMSSON, R
    DOKAL, I
    LUZZATTO, L
    CONNOR, JM
    [J]. JOURNAL OF MEDICAL GENETICS, 1993, 30 (07) : 618 - 619
  • [5] X-LINKED MYOTUBULAR MYOPATHY WITH FATAL NEONATAL ASPHYXIA
    BARTH, PG
    VANWIJNGAARDEN, GK
    BETHLEM, J
    [J]. NEUROLOGY, 1975, 25 (06) : 531 - 536
  • [6] OTOPALATODIGITAL SYNDROME TYPE-I - FURTHER EVIDENCE FOR ASSIGNMENT OF THE LOCUS TO XQ28
    BIANCALANA, V
    LEMAREC, B
    ODENT, S
    VANDENHURK, JAMJ
    HANAUER, A
    [J]. HUMAN GENETICS, 1991, 88 (02) : 228 - 230
  • [7] BIRNBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513
  • [8] EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING
    BUCKLER, AJ
    CHANG, DD
    GRAW, SL
    BROOK, JD
    HABER, DA
    SHARP, PA
    HOUSMAN, DE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) : 4005 - 4009
  • [9] ISOLATION OF GENES FROM COMPLEX SOURCES OF MAMMALIAN GENOMIC DNA USING EXON AMPLIFICATION
    CHURCH, DM
    STOTLER, CJ
    RUTTER, JL
    MURRELL, JR
    TROFATTER, JA
    BUCKLER, AJ
    [J]. NATURE GENETICS, 1994, 6 (01) : 98 - 105
  • [10] GENOMIC SEQUENCING
    CHURCH, GM
    GILBERT, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07): : 1991 - 1995