A new troponin T and cDNA clones for 13 different muscle proteins, found by shotgun sequencing
- 1 April 1983
- journal article
- Published by Springer Nature in Nature
- Vol. 302 (5910), 718-721
- https://doi.org/10.1038/302718a0
Abstract
Complete amino acid sequences have been established for 19 muscle-related proteins and these proteins are each sufficiently abundant to suggest that their mRNA levels are about 0.4% or higher. Based on these considerations, a simple theoretical analysis shows that clones for most of these proteins can be identified within a complementary DNA library by sequencing cDNA inserts from 150-200 randomly selected clones. This procedure should not only rigorously identify specific clones, but it could also uncover amino acid sequence variants of major muscle proteins such as the troponins. We have determined sequences for about 20,000 nucleotides within 178 randomly selected clones of a rabbit muscle cDNA library, and report here that in addition to finding sequences encoding the two known skeletal muscle isotypes of troponin C, we have discovered sequences encoding two forms of troponin T. Over the region of nucleotide sequence overlap in the troponin T clones, the new isotype diverges significantly from its counterpart. Altogether, clones for 13 of the 19 known muscle-specific proteins were identified, in addition to the clone for the new troponin T isotype.Keywords
This publication has 34 references indexed in Scilit:
- Nucleotide sequence and evolution of a mammalian α-Tubulin messenger RNAJournal of Molecular Biology, 1981
- Regulation of muscle differentiation: isolation and purification of chick actin messenger ribonucleic acid and quantitation with complementary deoxyribonucleic acid probesBiochemistry, 1980
- Troponin C from Rabbit Slow Skeletal and Cardiac Muscle Is the Product of a Single GeneEuropean Journal of Biochemistry, 1980
- Control of embryonic development: isolation and purification of chick heart myosin light chain mRNA and quantitation with a cDNA probeBiochemistry, 1979
- Parvalbumin from Rabbit Muscle. Isolation and Primary StructureEuropean Journal of Biochemistry, 1976
- Cyanogen bromide fragments of the cardiac I light chain from bovine myosin: Evidence for sequence homology with rabbit skeletal myosin alkali light chainsFEBS Letters, 1975
- The amino acid sequence of bovine cardiac troponin-C. Comparison with rabbit skeletal troponin-CBiochemical and Biophysical Research Communications, 1975
- Homology of myosin light chains, troponin-C and parvalbumins deduced from comparison of their amino acid sequencesBiochemical and Biophysical Research Communications, 1974
- The amino acid sequence of rabbit skeletal muscle troponin C: Gene replication and homology with calcium ‐binding proteins from carp and hake muscleFEBS Letters, 1973
- Regulation of muscle contraction. Effect of calcium on the affinity of troponin for actin and tropomyosinBiochemistry, 1973