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- Title
Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder.
- Authors
Bowen, T.; Norton, N.; Jacobsen, N.J.O.; Guy, C.; Daniels, J.K.; Sanders, R.D.; Cardno, A.G.; Jones, L.A.; Murphy, K.C.; McGuffin, P.; Craddock, N.; O'Donovan, M.C.; Owen, M.J.
- Abstract
The evidence for a significant genetic contribution to the functional psychoses (schizophrenia and bipolar disorder) is now well established. However, in both cases, the non-mendelian mode of inheritance has made the identification of susceptibility loci particularly challenging. The neuropeptide cholecystokinin (CCK) is present both in the gut and the CNS. Studies of CCKlike immunoreactivity and CCK mRNA levels in human brains have revealed high concentrations in numerous loci and shown colocalisation of CCK with, for example, dopamine and tyrosine hydroxylase. Furthermore, antagonists of CCK-B receptors, which are found most frequently in the brain, inhibit the activity of brain dopamine neurons. Such findings suggest that, with respect to neuropsychiatric disorders, CCK is a suitable candidate for analysis using methods to detect gene variations which have the potential to affect protein structure or expression. In the present study, mutation analyses were carried out on the human CCK gene. Linked polymorphisms were found in the promoter region and in intron 1 close to the 3' mRNA splice acceptor site. However, the allele frequencies of these polymorphisms in samples of individuals affected with either schizophrenia (n=117) or bipolar disorder (n=124) did not differ from those of control subjects (n=234), suggesting that these variations do not confer a predisposition to either of the functional psychoses.
- Subjects
GENETIC polymorphisms; EXONS (Genetics); CHOLECYSTOKININ
- Publication
Molecular Psychiatry, 1998, Vol 3, Issue 1, p67
- ISSN
1359-4184
- Publication type
Article
- DOI
10.1038/sj.mp.4000293