Assignment of the human pancreatic colipase gene to chromosome 6p21.1 to pter

R C Davis1, Y R Xia, T Mohandas

  • 1Lipid Research, VA Wadsworth Medical Center, Los Angeles, California 90073.

Genomics
|May 1, 1991
PubMed

Insights

Researchers identified the human colipase gene (CLPS) location using molecular techniques. This gene is crucial for pancreatic lipase function in dietary fat absorption.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Genetics

Background:

  • Pancreatic colipase is a vital cofactor for pancreatic lipase, facilitating dietary long-chain fatty acid absorption.
  • Colipase stabilizes lipase on lipid micelles, opposing bile salt interference during digestion.

Purpose of the Study:

  • To clone the complete coding region of human procolipase mRNA.
  • To determine the chromosomal location of the human colipase gene (CLPS).

Main Methods:

  • Polymerase chain reaction (PCR) was used to generate a cDNA clone of human procolipase mRNA.
  • Southern blot analysis of mouse-human somatic cell hybrids identified the gene's chromosome.
  • Analysis of translocation hybrids refined the gene's regional localization on chromosome 6.

Main Results:

  • A cDNA clone representing the full coding sequence of human procolipase mRNA was successfully produced.
  • The colipase gene (CLPS) was mapped to human chromosome 6.
  • CLPS was regionally localized to the 6p21.1-pter region of chromosome 6.

Conclusions:

  • The study successfully cloned human procolipase cDNA and localized the CLPS gene to chromosome 6p21.1-pter.
  • This provides a genetic basis for understanding colipase function and potential related disorders.

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