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Title

The human lanosterol synthase gene maps to chromosome 21q22.3

Authors
Young, M.
Chen, H.
Lalioti, M. D.
Published in Human Genetics. 1996, vol. 97, no. 5, p. 620-624
Abstract In order to contribute to the development of the transcriptional map of human chromosome 21 (HC21) we have used exon trapping to identify portions of HC21 genes. Using pools of random HC21-specific cosmids from the LL21NC02-Q library and cosmids from 21q22.3 we have identified five different coding regions with strong homology to the lanosterol synthase genes of rat and yeast. This enzyme catalyzes the cyclization of squalene-2,3-epoxide lanosterol, which is the parental compound of all steroids in mammals. Using somatic cell hybrids and HC21 yeast artificial chromosomes (YACS) and cosmids, we mapped the human lanosterol synthase cDNA gene to 2lq22.3 between markers D21S25 and 21qter. Cosmid Q7G8 from the LL21NC02-Q library and YAC 145D8 from the CEPH HC21 contig contain this human gene. We cloned a portion of the human lanosterol synthase cDNA (almost 85% of the coding region) from a brain cDNA library and determined its nucleotide sequence. The predicted human protein shows 83% identity to its rat and 40% to its yeast homolog. No obvious candidate human disease exists for lanosterol synthase deficiency and the role (if any) of triplication of this gene in the various phenotypes of trisomy 21 is unknown.
Keywords Amino Acid SequenceAnimalsBase SequenceBrain/enzymologyCandida albicans/enzymologyChromosome MappingChromosomes, Artificial, YeastChromosomes, Human, Pair 21Cloning, MolecularCosmidsDNA PrimersExonsGene LibraryHumansIntramolecular TransferasesIsomerases/biosynthesis/chemistry/ geneticsMolecular Sequence DataPolymerase Chain ReactionRandom AllocationRatsRecombinant Proteins/biosynthesis/chemistrySaccharomyces cerevisiae/enzymologySequence Homology, Amino Acid
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PMID: 8655142
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YOUNG, M. et al. The human lanosterol synthase gene maps to chromosome 21q22.3. In: Human Genetics, 1996, vol. 97, n° 5, p. 620-624. doi: 10.1007/bf02281872 https://archive-ouverte.unige.ch/unige:9106

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Deposited on : 2010-07-12

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