Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1996-9-25
pubmed:databankReference
pubmed:abstractText
We cloned the full-length rat leptin receptor (Ob-R) isoform complementary DNAs (cDNAs) and examined the gene expression in rats. We also identified a mutation in Ob-R in Zucker fatty (fa/fa) rats. Three alternatively spliced isoforms (Ob-Ra, Ob-Rb, and Ob-Re) have been identified, which are closely related to the gp130 signal-transduction component of class I cytokine receptors. Rat Ob-Ra and Ob-Rb were single transmembrane proteins, which differ in the C-terminal amino acid sequences. On the other hand, Ob-Re had no transmembrane domain and was a soluble form of the receptor. Reverse transcription-polymerase chain reaction analysis revealed that Ob-R isoform messenger RNAs (mRNAs) are expressed in a wide variety of rat tissues in tissue-specific manners. A missense mutation (an A to C conversion at nucleotide position 806) was found in the extracellular domain of all the isoforms in Zucker fatty (fa/fa) rats, which resulted in an amino acid change from Gln to Pro at + 269 (the Gln269Pro mutation). These Ob-R isoform mRNAs were present in the brain from Zucker fatty (fa/fa) rats at comparable amounts to those in their lean littermates. The present study provides new insight into the molecular mechanisms for Ob-R.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0006-291X
pubmed:author
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
225
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
75-83
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:8769097-Alternative Splicing, pubmed-meshheading:8769097-Amino Acid Sequence, pubmed-meshheading:8769097-Animals, pubmed-meshheading:8769097-Base Sequence, pubmed-meshheading:8769097-Carrier Proteins, pubmed-meshheading:8769097-Cloning, Molecular, pubmed-meshheading:8769097-DNA, Complementary, pubmed-meshheading:8769097-DNA Primers, pubmed-meshheading:8769097-Gene Expression, pubmed-meshheading:8769097-Humans, pubmed-meshheading:8769097-Male, pubmed-meshheading:8769097-Mice, pubmed-meshheading:8769097-Mice, Obese, pubmed-meshheading:8769097-Molecular Sequence Data, pubmed-meshheading:8769097-Obesity, pubmed-meshheading:8769097-Organ Specificity, pubmed-meshheading:8769097-Point Mutation, pubmed-meshheading:8769097-Polymerase Chain Reaction, pubmed-meshheading:8769097-RNA, Messenger, pubmed-meshheading:8769097-Rats, pubmed-meshheading:8769097-Rats, Sprague-Dawley, pubmed-meshheading:8769097-Rats, Zucker, pubmed-meshheading:8769097-Receptors, Cell Surface, pubmed-meshheading:8769097-Receptors, Cytokine, pubmed-meshheading:8769097-Receptors, Leptin, pubmed-meshheading:8769097-Sequence Homology, Amino Acid
pubmed:year
1996
pubmed:articleTitle
Molecular cloning of rat leptin receptor isoform complementary DNAs--identification of a missense mutation in Zucker fatty (fa/fa) rats.
pubmed:affiliation
Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Japan.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't