Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.

Published

Journal Article

In a systematic sequencing screen of the coding exons of the X chromosome in 250 families with X-linked mental retardation (XLMR), we identified two nonsense mutations and one consensus splice-site mutation in the AP1S2 gene on Xp22 in three families. Affected individuals in these families showed mild-to-profound mental retardation. Other features included hypotonia early in life and delay in walking. AP1S2 encodes an adaptin protein that constitutes part of the adaptor protein complex found at the cytoplasmic face of coated vesicles located at the Golgi complex. The complex mediates the recruitment of clathrin to the vesicle membrane. Aberrant endocytic processing through disruption of adaptor protein complexes is likely to result from the AP1S2 mutations identified in the three XLMR-affected families, and such defects may plausibly cause abnormal synaptic development and function. AP1S2 is the first reported XLMR gene that encodes a protein directly involved in the assembly of endocytic vesicles.

Full Text

Duke Authors

Cited Authors

  • Tarpey, PS; Stevens, C; Teague, J; Edkins, S; O'Meara, S; Avis, T; Barthorpe, S; Buck, G; Butler, A; Cole, J; Dicks, E; Gray, K; Halliday, K; Harrison, R; Hills, K; Hinton, J; Jones, D; Menzies, A; Mironenko, T; Perry, J; Raine, K; Richardson, D; Shepherd, R; Small, A; Tofts, C; Varian, J; West, S; Widaa, S; Yates, A; Catford, R; Butler, J; Mallya, U; Moon, J; Luo, Y; Dorkins, H; Thompson, D; Easton, DF; Wooster, R; Bobrow, M; Carpenter, N; Simensen, RJ; Schwartz, CE; Stevenson, RE; Turner, G; Partington, M; Gecz, J; Stratton, MR; Futreal, PA; Raymond, FL

Published Date

  • December 2006

Published In

Volume / Issue

  • 79 / 6

Start / End Page

  • 1119 - 1124

PubMed ID

  • 17186471

Pubmed Central ID

  • 17186471

International Standard Serial Number (ISSN)

  • 0002-9297

Digital Object Identifier (DOI)

  • 10.1086/510137

Language

  • eng

Conference Location

  • United States