Journal of Biological Chemistry · 1990 · 617 citations · 48 references
Life SciencesBiochemistryMolecular BiologyCell SignalingIon Channel BiophysicsStructural BiologyCalcium SignalingCalcium-binding ProteinsCardiac Ion ChannelsChannel StructureIon ChannelsProtein StructureAmino AcidsCalcium Ion SignalingCalcium-binding Site StructureHydropathy AnalysisMuscle Calcium TransportPhosphorylation Site MappingPhosphorylation Site PredictionRyanodine Receptors
We have cloned and sequenced cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. The cDNA, 16,532 base pairs in length, encodes a protein of 4,969 amino acids with a Mr of 564,711. The deduced amino acid sequence is 66% identical with that of the skeletal muscle ryanodine receptor, but analysis of predicted secondary structures and hydropathy plots suggests that the two isoforms exhibit the same topology in both transmembrane and cytoplasmic domains. A potential ATP binding domain was identified at residues 2619-2652, a potential phosphorylation site at residue 2809, and potential calmodulin binding sites at residues 2775-2807, 2877-2898, and 2998-3016. We suggest that a modulator binding domain in the protein lies between residues 2619 and 3016. Northern blot analysis of mRNA from a variety of tissues demonstrated that the cardiac isoform is expressed in heart and brain, while the skeletal muscle isoform is expressed in both fast- and slow-twitch muscle. No ryanodine receptor mRNA was detected in extracts from smooth muscle or any other non-muscle tissue examined. The two receptors are clearly the products of separate genes, and the gene encoding the cardiac muscle ryanodine receptor was localized to chromosome 1.
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Molecular Cloning. A Laboratory Manual
EJ Wood · Biochemical Education · 1983 · 30.6K citations
Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
Randall K. Saiki, David H. Gelfand, Susanne Stoffel et al. · Science · 1988 · 17.2K citations