Characterization and chromosomal localization of the human homologue of a rat AMP-activated protein kinase-encoding gene: a major regulator of lipid metabolism in mammals
Autor: | James Scott, Nurul H. Sarkar, Kripamoy Aguan, Chee Gee See |
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Rok vydání: | 1994 |
Předmět: |
Molecular Sequence Data
Saccharomyces cerevisiae AMP-Activated Protein Kinases Protein Serine-Threonine Kinases Biology Polymerase Chain Reaction Homology (biology) Open Reading Frames AMP-activated protein kinase Multienzyme Complexes Complementary DNA Genetics Animals Humans Amino Acid Sequence Protein kinase A Gene Gene Library Mammals Base Sequence Sequence Homology Amino Acid Myocardium Chromosome Mapping AMPK Hominidae General Medicine Plants Lipid Metabolism Molecular biology Rats Open reading frame Liver Chromosomes Human Pair 1 biology.protein Hordeum vulgare Protein Kinases |
Zdroj: | Gene. 149:345-350 |
ISSN: | 0378-1119 |
Popis: | AMP-activated protein kinase (AMPK) phosphorylates and inactivates acetyl-CoA carboxylase and beta-hydroxy beta-methylglutaryl-coenzyme A (HMG-CoA) reductase which are the major enzymes involved in fatty acid and lipid biosyntheses. The AMPK gene from rat (rAMPK) has recently been cloned [Carling et al., J. Biol. Chem. 269 (1994) 11442-11448]. In order to study the structure and function of the human AMPK gene (hAMPK), we have cloned the gene, and report in this communication its nucleotide (nt) sequence, tissue distribution and chromosomal location. Our results show that the ORF of hAMPK encodes 552 amino acids (aa) (62.250 kDa) and is highly conserved with rAMPK with identities of 97.3 and 90% at the aa and nt levels, respectively. The hAMPK gene bears homology to a yeast protein kinase-encoding gene (snf1) that regulates carbohydrate metabolism, and also with three other genes encoding SNF1-like kinases from different plant species, namely Arabidopsis thaliana, Hordeum vulgare and Secale cereale. As determined by fluorescent in situ hybridization of a human metaphase chromosome spread, hAMPK maps to chromosome 1p31. The size of the hAMPK transcript is 8.5 kb and the transcription start point (tsp) is located approx. 46 bp upstream from the ATG codon. While 10-15% of AMPK is alternatively spliced in most tissues of the rat, our RT-PCR analyses of the hAMPK mRNA did not reveal the presence of any alternatively spliced form of the gene in human tissues. An interesting aspect of AMPK is that its expression, unlike in rat liver, could not be detected in human liver, and thus the purported role of the gene in controlling fatty-acid synthesis in the human liver remains to be determined. |
Databáze: | OpenAIRE |
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