The sucrase-isomaltase complex: primary structure, membrane-orientation, and evolution of a stalked, intrinsic brush border protein
W Hunziker, M Spiess, G Semenza, HF Lodish - Cell, 1986 - Elsevier
W Hunziker, M Spiess, G Semenza, HF Lodish
Cell, 1986•ElsevierThe complete primary structure (1827 amino acids) of rabbit intestinal pro-sucrase-
isomaltase (pro-SI) was deduced from the sequence of a nearly full-length cDNA. Pro-SI is
anchored in the membrane by a single 20 amino acid segment spanning the bilayer only
once. The amino-terminal, cytoplasmic domain consists of 12 amino acids and is not
preceded by a cleaved leader sequence. This suggests a dual role for the membrane-
spanning segment as an uncleaved signal for membrane insertion. This is followed by a 22 …
isomaltase (pro-SI) was deduced from the sequence of a nearly full-length cDNA. Pro-SI is
anchored in the membrane by a single 20 amino acid segment spanning the bilayer only
once. The amino-terminal, cytoplasmic domain consists of 12 amino acids and is not
preceded by a cleaved leader sequence. This suggests a dual role for the membrane-
spanning segment as an uncleaved signal for membrane insertion. This is followed by a 22 …
Abstract
The complete primary structure (1827 amino acids) of rabbit intestinal pro-sucrase-isomaltase (pro-SI) was deduced from the sequence of a nearly full-length cDNA. Pro-SI is anchored in the membrane by a single 20 amino acid segment spanning the bilayer only once. The amino-terminal, cytoplasmic domain consists of 12 amino acids and is not preceded by a cleaved leader sequence. This suggests a dual role for the membrane-spanning segment as an uncleaved signal for membrane insertion. This is followed by a 22 residue serine/threonine-rich, probably glycosylated, stretch, presumably forming the stalk on which the globular, catalytic domains are directed into the intestinal lumen. Following this is a high degree of homology between the isomaltase and sucrase portions (41% amino acid identity), indicating that pro-SI evolved by partial gene duplication.
Elsevier