Format

Send to:

Choose Destination
See comment in PubMed Commons below
Pharmacogenet Genomics. 2006 Jul;16(7):461-8.

Naturally occurring mutation Leu307Pro of human butyrylcholinesterase in the Vysya community of India.

Author information

  • 1Bharathiar University, Department of Biotechnology, Coimbatore, Tamil Nadu, India.

Abstract

BACKGROUND:

People with genetic variants of butyrylcholinesterase (EC 3.1.1.8, BChE) can have hours of prolonged apnea after a normal dose of succinylcholine or mivacurium.

METHODS:

Plasma samples from 226 people in the Vysya community in Coimbatore, India were tested for BChE activity.

RESULTS:

Nine unrelated individuals had no detectable activity. DNA sequencing revealed a novel mutation in exon 2 of the BCHE gene, responsible for the silent phenotype of human serum BChE. All silent BChE samples were homozygous for a point mutation at codon 307 (CTT-->CCT), resulting in substitution of leucine 307 by proline. Western blot analysis with a monoclonal antibody showed no BChE protein in plasma. Silent BChE plasma samples had no organophosphate-reactive BChE, as measured with FP-biotin. Expression of recombinant Leu307Pro BChE in cell culture confirmed that this mutant is expressed at very low levels. The proline substitution most likely destabilizes the BChE structure and causes the protein to be misfolded and rapidly degraded.

CONCLUSIONS:

This is the first report of a molecularly defined BChE mutation in the Indian population. The frequency of homozygous silent BChE in the Vysya community is 1 in 24, a value 4000-fold higher than the frequency of homozygous silent BChE in European and American populations.

PMID:
16788378
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Lippincott Williams & Wilkins
    Loading ...
    Write to the Help Desk