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Structure of the human pancreatic cholesterol esterase gene

Authors :
Louis G. Lange
Jose A. Aleman-Gomez
Matthew S. Bosner
Kumar Bv
Niall S. Colwell
C. A. Spilburg
Mark E. Lowe
Lopez-Candales A
Source :
Biochemistry. 31:6077-6081
Publication Year :
1992
Publisher :
American Chemical Society (ACS), 1992.

Abstract

The gene for human pancreatic cholesterol esterase consists of 11 exons and 10 introns and is 9.2 kb in length. The last and longest exon (841 nucleotides) is unique to the human gene. Functional amino acids are encoded on separate exons. The leader sequence is encoded by a single exon which carries two additional N-terminal amino acids of the mature functional protein. A positive TATA element is identified 43 nucleotides from the start codon. Pulse-field gel electrophoresis and hybridization with various cDNA probes and direct sequence data revealed the existence of a CEase-like gene. Partial sequence analysis of this gene from a human cosmid library and human genomic DNA showed a premature stop signal in exon 10, shortly after the codon for the active-site histidine. Both the functional gene and the CEase-like gene have a polyadenylation signal in the 3'-untranslated region. Thus, the complex gene structure for this intestinally active enzyme may provide in part a potential molecular explanation for the well-known heterogeneity of the intestinal absorption of cholesterol.

Details

ISSN :
15204995 and 00062960
Volume :
31
Database :
OpenAIRE
Journal :
Biochemistry
Accession number :
edsair.doi.dedup.....b271e0635e0b9067ff5282ab7ab354a8
Full Text :
https://doi.org/10.1021/bi00141a017