A HUMAN SYNAPTIC VESICLE MONOAMINE TRANSPORTER CDNA PREDICTS POSTTRANSLATIONAL MODIFICATIONS, REVEALS CHROMOSOME-10 GENE LOCALIZATION AND IDENTIFIES TAQI RFLPS

被引:72
|
作者
SURRATT, CK
PERSICO, AM
YANG, XD
EDGAR, SR
BIRD, GS
HAWKINS, AL
GRIFFIN, CA
LI, X
JABS, EW
UHL, GR
机构
[1] NIDA,ADDICT RES CTR,BOX 5180,BALTIMORE,MD 21224
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,CTR ONCOL,DEPT NEUROSCI,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
[5] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205
关键词
MONOAMINE TRANSPORTER; CHROMOSOMAL MAPPING; POLYMORPHISM; N-LINKED GLYCOSYLATION;
D O I
10.1016/0014-5793(93)80539-7
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
A human vesicular monoamine transporter cDNA has been identified by screening a human brainstem library using sequences from the rat brain synaptic vesicle monoamine transporter (SVMT) [(1992) Cell 70, 539-55 1; (1992) Proc. Natl. Acad. Sci. USA 89,10993-109971. The hSVMT shares 92% amino acid identity with the rat sequence, but displays one less consensus site for asparagine N-linked glycosylation and one more consensus site for phosphorylation by protein kinase C. The human SVMT gene maps to chromosome 10q25 using Southern blotting analysis of human/rodent hybrid cell lines and fluorescent in situ hybridization approaches. The cDNA, and a subclone, recognize TaqI polymorphisms that may prove useful to assess this gene's involvement in neuropsychiatric disorders involving monoaminergic brain systems.
引用
收藏
页码:325 / 330
页数:6
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