QM is a human cDNA originally isolated as a transcript elevated in a nontumorigenic Wilms' tumor microcell hybrid, relative to the tumorigenic parental cell line. The QM gene encodes a 24 kDa basic protein that peripherally associates with the ribosomes. Recently, the gene for this protein has also
Synthesis and turnover of ribosomal proteins in the absence of 60S subunit assembly in Saccharomyces cerevisiae
β Scribed by Gorenstein, Charles ;Warner, Jonathan R.
- Publisher
- Springer
- Year
- 1977
- Tongue
- English
- Weight
- 472 KB
- Volume
- 157
- Category
- Article
- ISSN
- 0026-8925
No coin nor oath required. For personal study only.
β¦ Synopsis
We have measured the synthesis and stability of ribosomal proteins in a temperature sensitive strain of yeast which at the restrictive temperature is specifically blocked in the processing of 27S ribosomal precursor RNA. We find that in the absence of 60S ribosomal subunit assembly, the synthesis of all the ribosomal proteins studied continued. However, the proteins of the 60S subunit fail to accumulate and are rapidly degraded.
π SIMILAR VOLUMES
## Abstract The synthesis of ribosomes in HeLa cells was studied during recovery from a 20βhour deprivation for valine. The rates of incorporation of labeled precursors into ribosomal preβRNA, processed rRNA, total cellular proteins, and proteins of the 60S ribosomal subunit returned to normal or n
In the above paper (Yeast 11: 761-766 (1995)) ribosomal protein L17a is erroneously referred to as L17, which is a ribosomal protein distinct from L17a. All references to the products of the RPL 17A and RPL 17B genes should be L 17a.
The peptide-chain elongation rate of Saccharomyces cerevisiae at two different growth rates was estimated by the kinetics of radioactive labelling of nascent and finished polypeptides as described by Gausing, 1972, and Young and Bremer, 1976. The elongation rates of a diploid strain cultured in yeas