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Cleavage within an RNase III site can control mRNA stability and protein synthesis in vivo.

We report that processing at a cloned bacteriophage T7 RNase III site results in strong stabilization of the mRNA relative to the full-length transcript. In contrast, processing by RNase III of the bacteriophage lambda int transcript leads to rapid degradation of the messenger. It is proposed that t...

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Bibliografske podrobnosti
Main Authors: Panayotatos, N, Truong, K
Format: Artigo
Jezik:Inglês
Izdano: 1985
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC341151/
https://ncbi.nlm.nih.gov/pubmed/2987846
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