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Ultracentrifuge studies of RNA degradation

Archives of Biochemistry and Biophysics, 1962
Ultracentrifuge studies of RNA from Ehrlich ascites cells have shown that the original 28, 18, and 3–5 S components change progressively as a result of degradation. The 28 S component diminishes at a much more rapid rate than the 18 S, and their relative ratio changes as a function of the age of the RNA samples. Intermediary components of 24, 21, 15,
J, HUPPERT, J, PELMONT
openaire   +2 more sources

On the degradation of intracellular RNA by ribonucleases

International Journal of Biochemistry, 1986
The kinetic and the specificity of two RNases purified from the insect. C. capitata have been studied. These two enzymes exhibit preference to degrade large polynucleotides. The alkaline enzyme is located in the soluble cellular fraction and the acid enzyme is also associated to microsomes and lysosomes.
Jvan M. Garcia-Segura   +4 more
openaire   +2 more sources

Polyadenylation and degradation of RNA in the mitochondria

Biochemical Society Transactions, 2016
Mitochondria have their own gene expression machinery and the relative abundance of RNA products in these organelles in animals is mostly dictated by their rate of degradation. The molecular mechanisms regulating the differential accumulation of the transcripts in this organelle remain largely elusive.
Shiri, Levy, Gadi, Schuster
openaire   +2 more sources

Maturation and degradation of RNA in bacteria

Current Opinion in Microbiology, 2007
RNA decay plays an important role, not only in recycling nucleotides but also in determining the rapidity with which cells can react to changing growth conditions. The degradation process can be regulated, thus providing an often-underestimated means of controlling gene expression. Recent developments in the field of RNA maturation and decay in two key
openaire   +3 more sources

Degradation of circular RNA by the ribonuclease DIS3

Molecular Cell
Features of circular RNAs (circRNAs) produced by back-splicing of eukaryotic exon(s) make them resistant to degradation by linear RNA decay machineries. Thus, a general circRNA degradation pathway under normal conditions has remained largely elusive.
Ling-Ling Chen   +2 more
exaly   +3 more sources

Messenger RNA degradation in Saccharomyces cerevisiae

Gene, 1988
The analysis of 17 functional mRNAs and two recombinant mRNAs in the yeast Saccharomyces cerevisiae suggests that the length of an mRNA influences its half-life in this organism. The mRNAs are clearly divisible into two populations when their lengths and half-lives are compared.
A J, Brown   +5 more
openaire   +2 more sources

Direction of in vivo Degradation of a Messenger RNA

Nature, 1968
Degradation begins at the 3′ end of a trp, mRNA molecule and progresses sequentially to the 5′ end.
R F, Baker, C, Yanofsky
openaire   +2 more sources

High-fidelity Cas13 variants for targeted RNA degradation with minimal collateral effects

bioRxiv, 2021
Huawei Tong   +22 more
semanticscholar   +1 more source

Degradation of RNA in Escherichia coli

Molecular and General Genetics MGG, 1973
A hypothesis to explain RNA degradation in Escherichia coli is proposed. In this hypothesis all classes of RNA are potentially degradable unless they are protected. The proposed mechanism for mRNA degradation requires a combination of endonuclease(s) and exonuclease(s) which degrades RNA in the 3′ to 5′ direction.
openaire   +2 more sources

Linking circular intronic RNA degradation and function in transcription by RNase H1

Science China Life Sciences, 2021
Xiang Li   +11 more
semanticscholar   +1 more source

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