Systematic discovery of cap-independent translation sequences in human and viral genomes

Author:

Weingarten-Gabbay Shira12,Elias-Kirma Shani12,Nir Ronit12,Gritsenko Alexey A.345,Stern-Ginossar Noam6,Yakhini Zohar78,Weinberger Adina12,Segal Eran12

Affiliation:

1. Department of Computer Science and Applied Mathematics, Weizmann Institute of Science, Rehovot 76100, Israel.

2. Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel.

3. The Delft Bioinformatics Laboratory, Department of Intelligent Systems, Delft University of Technology, Delft, Netherlands.

4. Platform Green Synthetic Biology, Delft, Netherlands.

5. Kluyver Centre for Genomics of Industrial Fermentation, Delft, Netherlands.

6. Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.

7. Department of Computer Science, Technion, Haifa, Israel.

8. Agilent Laboratories, Tel-Aviv, Israel.

Abstract

Identifying the IRESs of humans and viruses Most proteins result from the translation of 5′ capped RNA transcripts. In viruses and a subset of human genes, RNA transcripts with internal ribosome entry sites (IRESs) are uncapped. Weingarten-Gabbay et al. systematically surveyed the presence of IRESs in human protein-coding transcripts, as well those of viruses (see the Perspective by Gebauer and Hentze). Large-scale mutagenesis profiling identified two classes of IRESs: those having a functional element localized to one small region of the IRES and those with important elements distributed across the entire region. An unbiased screen across human genes suggests that IRESs are more frequent than previously supposed in 3′ untranslated regions. Science , this issue p. 10.1126/science.aad4939 ; see also p. 228

Funder

NIH

European Research Council (ERC)

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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