THE HUMAN CATIONIC AMINO-ACID TRANSPORTER (ATRC1) - PHYSICAL AND GENETIC-MAPPING TO 13Q12-Q14

被引:39
作者
ALBRITTON, LM
BOWCOCK, AM
EDDY, RL
MORTON, CC
TSENG, L
FARRER, LA
CAVALLISFORZA, LL
SHOWS, TB
CUNNINGHAM, JM
机构
[1] BRIGHAM & WOMENS HOSP, HOWARD HUGHES MED INST, BOSTON, MA 02115 USA
[2] STANFORD UNIV, SCH MED, DEPT GENET, PALO ALTO, CA 94305 USA
[3] BOSTON UNIV, SCH MED, DEPT NEUROL, BOSTON, MA 02118 USA
[4] NEW YORK STATE DEPT HLTH, ROSWELL PK MEM INST, DEPT HUMAN GENET, BUFFALO, NY 14263 USA
[5] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
[6] BRIGHAM & WOMENS HOSP, DEPT MED, DIV HEMATOL, BOSTON, MA 02115 USA
[7] BRIGHAM & WOMENS HOSP, DEPT PATHOL, BOSTON, MA 02115 USA
关键词
D O I
10.1016/0888-7543(92)90431-Q
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 product of the mouse Rec-1 locus is an integral membrane protein that determines susceptibility to infection by murine ecotropic retroviruses. Recently it has been determined that its role in normal cell metabolism is transport of the cationic amino acids, arginine, lysine, and ornithine across the plasma membrane. Southern blot analysis of genomic DNA from a panel of 48 mouse-human somatic cell hybrids assigned the human version of this gene, ATRC1, to chromosome 13. Chromosomal in situ hybridization localized the gene to 13q12-q14. A restriction fragment length polymorphism (RFLP) was detected with TaqI. There were two alleles with frequencies of 0.29 and 0.71. Pairwise linkage analysis established linkage between ATRC1 and ATP1AL1, D13S1, D13S6, D13S10, D13S11, D13S21, D13S22, D13S33, D13S36, and D13S37. Multilocus linkage analysis of five of the loci indicated that the most likely order of loci in this region was D13S11-ATP1AL1-ATRC1-D13S6-D13S33. © 1992.
引用
收藏
页码:430 / 434
页数:5
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