Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons
Tryptophan hydroxylase isoform 2 (TPH2) is expressed in serotonergic neurons in the raphe nuclei, where it catalyzes the rate-limiting step in the synthesis of the neurotransmitter serotonin. In search for functional polymorphisms within the TPH2 gene locus, we measured allele-specific expression of...
Saved in:
Published in | Molecular psychiatry Vol. 12; no. 5; pp. 491 - 501 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.05.2007
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Tryptophan hydroxylase isoform 2 (TPH2) is expressed in serotonergic neurons in the raphe nuclei, where it catalyzes the rate-limiting step in the synthesis of the neurotransmitter serotonin. In search for functional polymorphisms within the
TPH2
gene locus, we measured allele-specific expression of
TPH2
mRNA in sections of human pons containing the dorsal and median raphe nuclei. Differences in allelic mRNA expression – referred to as allelic expression imbalance (AEI) – are a measure of
cis
-acting regulation of gene expression and mRNA processing. Two marker SNPs, located in exons 7 and 9 of
TPH2
(rs7305115 and rs4290270, respectively), served for quantitative allelic mRNA measurements in pons RNA samples from 27 individuals heterozygous for one or both SNPs. Significant AEI (ranging from 1.2- to 2.5-fold) was detected in 19 out of the 27 samples, implying the presence of
cis
-acting polymorphisms that differentially affect
TPH2
mRNA levels in pons. For individuals heterozygous for both marker SNPs, the results correlated well (
r
=0.93), validating the AEI analysis. AEI is tightly associated with the exon 7 marker SNP, in 17 of 18 subjects. Remarkably, expression from the minor allele exceeded that of the major allele in each case, possibly representing a gain-of-function. Genotyping of 20 additional
TPH2
SNPs identified a haplotype block of five tightly linked SNPs for which heterozygosity is highly correlated with AEI and overall expression of
TPH2
mRNA. These results reveal the presence of a functional
cis
-acting polymorphism, with high frequency in normal human subjects, resulting in increased
TPH2
expression levels. The SNPs that correlate with AEI are closely linked to
TPH2
SNPs previously shown to associate with major depression and suicide. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1359-4184 1476-5578 |
DOI: | 10.1038/sj.mp.4001923 |