MAPPING OF 2 PHENOL SULFOTRANSFERASE GENES, STP AND STM, TO 16P - CANDIDATE GENES FOR BATTEN-DISEASE

被引:37
作者
DOOLEY, TP
MITCHISON, HM
MUNROE, PB
PROBST, P
NEAL, M
SICILIANO, MJ
DENG, ZM
DOGGETT, NA
CALLEN, DF
GARDINER, RM
MOLE, SE
机构
[1] UNIV LONDON,SCH MED,RAYNE INST,DEPT PAEDIAT,LONDON WC1E 6JJ,ENGLAND
[2] SW FDN BIOMED RES,DEPT GENET,SAN ANTONIO,TX
[3] MD ANDERSON CANC CTR,DEPT MOLEC GENET,HOUSTON,TX
[4] LOS ALAMOS NATL LAB,DIV LIFE SCI,LOS ALAMOS,NM
[5] LOS ALAMOS NATL LAB,CTR HUMAN GENOME STUDIES,LOS ALAMOS,NM 87545
[6] ADELAIDE CHILDRENS HOSP INC,DEPT CYTOGENET & MOLEC GENET,ADELAIDE,SA,AUSTRALIA
关键词
D O I
10.1006/bbrc.1994.2691
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cytosolic phenol sulphotransferase gene (STP) was mapped to a region of chromosome 16, within the interval defined by human-rodent somatic cell hybrid breakpoints CY160(D) and CY12, which contains FRA16E. YAC and cosmid clones from this 16p interval were screened for the presence of STP. Two non-overlapping cosmid contigs were identified which contain STP-like sequences. Sequencing of these STP-like sequences confirmed that STP is contained within contig 343.1 and maps proximal to FRA16E, and that a related sulphotransferase STM,encoding the catecholamine-sulphating enzyme, is contained within contig 55.4 and maps to the adjacent hybrid interval CY12-CY180A. Thus two phenol sulphotransferase genes (STP and STM) have been finely localised to chromosome 16p12.1-p11.2, to the same region as CLN3, the gene for Batten disease. Both genes are therefore candidate genes for Batten disease. (C) 1994 Academic Press, Inc.
引用
收藏
页码:482 / 489
页数:8
相关论文
共 23 条
  • [1] HIGH-RESOLUTION CYTOGENETIC-BASED PHYSICAL MAP OF HUMAN CHROMOSOME-16
    CALLEN, DF
    DOGGETT, NA
    STALLINGS, RL
    CHEN, LZ
    WHITMORE, SA
    LANE, SA
    NANCARROW, JK
    APOSTOLOU, S
    THOMPSON, AD
    LAPSYS, NM
    EYRE, HJ
    BAKER, EG
    SHEN, Y
    HOLMAN, K
    PHILLIPS, H
    RICHARDS, RI
    SUTHERLAND, GR
    [J]. GENOMICS, 1992, 13 (04) : 1178 - 1185
  • [2] HUMAN-LIVER PHENOL SULFOTRANSFERASE - ASSAY CONDITIONS, BIOCHEMICAL-PROPERTIES AND PARTIAL-PURIFICATION OF ISOZYMES OF THE THERMOSTABLE FORM
    CAMPBELL, NRC
    VANLOON, JA
    WEINSHILBOUM, RM
    [J]. BIOCHEMICAL PHARMACOLOGY, 1987, 36 (09) : 1435 - 1446
  • [3] MAPPING OF THE PHENOL SULFOTRANSFERASE GENE (STP) TO HUMAN-CHROMOSOME 16P12.1-P11.2 AND TO MOUSE CHROMOSOME-7
    DOOLEY, TP
    OBERMOELLER, RD
    LEITER, EH
    CHAPMAN, HD
    FALANY, CN
    DENG, ZM
    SICILIANO, MJ
    [J]. GENOMICS, 1993, 18 (02) : 440 - 443
  • [4] MOLECULAR ENZYMOLOGY OF HUMAN LIVER CYTOSOLIC SULFOTRANSFERASES
    FALANY, CN
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1991, 12 (07) : 255 - 259
  • [5] PURIFICATION AND CHARACTERIZATION OF HUMAN LIVER PHENOL-SULFATING PHENOL SULFOTRANSFERASE
    FALANY, CN
    VAZQUEZ, ME
    HEROUX, JA
    ROTH, JA
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 278 (02) : 312 - 318
  • [6] JARVELA IE, 1995, UNPUB AM J MED GENET
  • [7] KOZMAN HM, 1994, IN PRESS GENOMICS
  • [8] MOLECULAR ANALYSIS OF HUMAN CHROMOSOME-16 COSMID CLONES CONTAINING NOTI SITES
    LERNER, T
    WRIGHT, G
    LEVERONE, B
    DACKOWSKI, W
    SHOOK, D
    ANDERSON, MA
    KLINGER, K
    CALLEN, D
    LANDES, G
    [J]. MAMMALIAN GENOME, 1992, 3 (02) : 92 - 100
  • [9] LERNER TJ, 1994, AM J HUM GENET, V54, P88
  • [10] FINE GENETIC-MAPPING OF THE BATTEN DISEASE LOCUS (CLN3) BY HAPLOTYPE ANALYSIS AND DEMONSTRATION OF ALLELIC ASSOCIATION WITH CHROMOSOME-16P MICROSATELLITE LOCI
    MITCHISON, HM
    THOMPSON, AD
    MULLEY, JC
    KOZMAN, HM
    RICHARDS, RI
    CALLEN, DF
    STALLINGS, RL
    DOGGETT, NA
    ATTWOOD, J
    MCKAY, TR
    SUTHERLAND, GR
    GARDINER, RM
    [J]. GENOMICS, 1993, 16 (02) : 455 - 460