Mutations in mental retardation

Mutations in the gene encoding a receptor for angiotensin II are found in patients with X-linked mental retardation.

Jonathan Weitzman(
Jul 2, 2002

The genetic and molecular basis of mental retardation, which may affect up to 3% of the human population, is unclear. In the 28 June Science, Virginie Vervoort and colleagues report that mutations in the AGTR2 gene, encoding the angiotensin II receptor may affect cognitive function in people with X-linked mental retardation (XLMR). Linkage analysis of XLMR families suggested that the Xq23-25 region might contain more than one gene related to the disease (Science 2002, 296:2401-2403).

Vervoort et al. studied translocation breakpoints in a female patient with mild retardation (with an IQ of 44); they examined expression of several candidate genes in the breakpoint region and found that the AGTR2 gene was silenced. They then screened affected males in several XLMR families and found one with a mutation in the AGTR2 gene that results in a truncated protein. Additional retardation patients with were also found AGTR2...

Interested in reading more?

Become a Member of

Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member?