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PMID: 12692552 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders.

Nature genetics ·Vol. 34 ·No. 1 ·2003-05-00 ·Pages 29-31

Jones B, Jones EL, Bonney SA, Patel HN, Mensenkamp AR, Eichenbaum-Voline S, Rudling M, Myrdal U, Annesi G, Naik S, Meadows N, Quattrone A, Islam SA, Naoumova RP, Angelin B, Infante R, Levy E, Roy CC, Freemont PS, Scott J, Shoulders CC

Abstract

Dietary fat is an important source of nutrition. Here we identify eight mutations in SARA2 that are associated with three severe disorders of fat malabsorption. The Sar1 family of proteins initiates the intracellular transport of proteins in COPII (coat protein)-coated vesicles. Our data suggest that chylomicrons, which vastly exceed the size of typical COPII vesicles, are selectively recruited by the COPII machinery for transport through the secretory pathways of the cell.

MeSH Terms
COP-Coated Vesicles/enzymology Chylomicrons/metabolism Dietary Fats/pharmacokinetics Female GTP Phosphohydrolases/chemistry,genetics Glycogen Storage Disease Type IV/enzymology,genetics Humans Intestinal Absorption Malabsorption Syndromes/enzymology,genetics,metabolism Male Models, Molecular Mutation Pedigree Protein Conformation Spinocerebellar Degenerations/enzymology,genetics
Chemicals
Chylomicrons Dietary Fats GTP Phosphohydrolases
Authors & Affiliations
21 authors, click to expand affiliations / ORCID
Jones Bethan
Genomic & Molecular Medicine Group, MRC Clinical Sciences Centre, Imperial College, London, England, UK.
Jones Emma L
Bonney Stephanie A
Patel Hetal N
Mensenkamp Arjen R
Eichenbaum-Voline Sophie
Rudling Mats
Myrdal Urban
Annesi Grazia
Naik Sandhia
Meadows Nigel
Quattrone Aldo
Islam Suhail A
Naoumova Rossitza P
Angelin Bo
Infante Recaredo
Levy Emile
Roy Claude C
Freemont Paul S
Scott James
Shoulders Carol C
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
2003-05-00
Pages
29-31
Language
English
Region
United States
NLM ID
9216904
Subset
IM
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