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 [J].
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 .
GENOMICS, 1992, 13 (04) :1178-1185
[2]   HUMAN-LIVER PHENOL SULFOTRANSFERASE - ASSAY CONDITIONS, BIOCHEMICAL-PROPERTIES AND PARTIAL-PURIFICATION OF ISOZYMES OF THE THERMOSTABLE FORM [J].
CAMPBELL, NRC ;
VANLOON, JA ;
WEINSHILBOUM, RM .
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 [J].
DOOLEY, TP ;
OBERMOELLER, RD ;
LEITER, EH ;
CHAPMAN, HD ;
FALANY, CN ;
DENG, ZM ;
SICILIANO, MJ .
GENOMICS, 1993, 18 (02) :440-443
[4]   MOLECULAR ENZYMOLOGY OF HUMAN LIVER CYTOSOLIC SULFOTRANSFERASES [J].
FALANY, CN .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1991, 12 (07) :255-259
[5]   PURIFICATION AND CHARACTERIZATION OF HUMAN LIVER PHENOL-SULFATING PHENOL SULFOTRANSFERASE [J].
FALANY, CN ;
VAZQUEZ, ME ;
HEROUX, JA ;
ROTH, JA .
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 [J].
LERNER, T ;
WRIGHT, G ;
LEVERONE, B ;
DACKOWSKI, W ;
SHOOK, D ;
ANDERSON, MA ;
KLINGER, K ;
CALLEN, D ;
LANDES, G .
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 [J].
MITCHISON, HM ;
THOMPSON, AD ;
MULLEY, JC ;
KOZMAN, HM ;
RICHARDS, RI ;
CALLEN, DF ;
STALLINGS, RL ;
DOGGETT, NA ;
ATTWOOD, J ;
MCKAY, TR ;
SUTHERLAND, GR ;
GARDINER, RM .
GENOMICS, 1993, 16 (02) :455-460