No evidence for SEL1L as a candidate gene for IDDM11-conferred susceptibility

Citation
F. Pociot et al., No evidence for SEL1L as a candidate gene for IDDM11-conferred susceptibility, DIABET M R, 17(4), 2001, pp. 292-295
Citations number
24
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
DIABETES-METABOLISM RESEARCH AND REVIEWS
ISSN journal
15207552 → ACNP
Volume
17
Issue
4
Year of publication
2001
Pages
292 - 295
Database
ISI
SICI code
1520-7552(200107/08)17:4<292:NEFSAA>2.0.ZU;2-U
Abstract
Background The SEL1L gene is located on human chromosome 14q24.3-31 close t o D14S67 which has been previously proposed to be a type 1 diabetes mellitu s locus (IDDM11). Sel-1 is a negative regulator of the Notch signalling pat hway and SEL1L is selectively expressed in adult pancreas and islets of Lan gerhans. This suggests that SEL1L may be a candidate gene for IDDM11. Methods We have analysed two newly identified CA-repeat polymorphisms withi n the genomic sequence of the SEL1L locus for association with type 1 diabe tes mellitus (T1DM) in 152 Danish T1DM-affected sib-pair families and in 24 0 Sardinian families (229 simplex and 11 sib-pair families). Results No evidence for association of the two SEL1L markers with T1DM was observed in either the Danish or the Sardinian families. We have also used allelic sharing methods to analyse linkage with T1DM in the IDDM11 region u sing the same markers and the Danish collection of affected sib-pair famili es. No evidence of linkage was observed (Z(max) = 0.86). Conclusion Although several lines of evidence suggest that SEL1L might be a candidate for IDDM11-conferred susceptibility to T1DM the present study do es not support this hypothesis. Copyright (C) 2001 John Wiley & Sons, Ltd.