Literature DB >> 31213602

CAPRI enables comparison of evolutionarily conserved RNA interacting regions.

Amol Panhale1, Florian M Richter1, Fidel Ramírez1, Maria Shvedunova1, Thomas Manke1, Gerhard Mittler2, Asifa Akhtar3.   

Abstract

RNA-protein complexes play essential regulatory roles at nearly all levels of gene expression. Using in vivo crosslinking and RNA capture, we report a comprehensive RNA-protein interactome in a metazoan at four levels of resolution: single amino acids, domains, proteins and multisubunit complexes. We devise CAPRI, a method to map RNA-binding domains (RBDs) by simultaneous identification of RNA interacting crosslinked peptides and peptides adjacent to such crosslinked sites. CAPRI identifies more than 3000 RNA proximal peptides in Drosophila and human proteins with more than 45% of them forming new interaction interfaces. The comparison of orthologous proteins enables the identification of evolutionary conserved RBDs in globular domains and intrinsically disordered regions (IDRs). By comparing the sequences of IDRs through evolution, we classify them based on the type of motif, accumulation of tandem repeats, conservation of amino acid composition and high sequence divergence.

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Year:  2019        PMID: 31213602      PMCID: PMC6581911          DOI: 10.1038/s41467-019-10585-3

Source DB:  PubMed          Journal:  Nat Commun        ISSN: 2041-1723            Impact factor:   14.919


  84 in total

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2.  Extended disordered regions of ribosome-associated NAC proteins paralogs belong only to the germline in Drosophila melanogaster.

Authors:  Galina L Kogan; Elena A Mikhaleva; Oxana M Olenkina; Sergei S Ryazansky; Oxana V Galzitskaya; Yuri A Abramov; Toomas A Leinsoo; Natalia V Akulenko; Sergey A Lavrov; Vladimir A Gvozdev
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7.  In vivo discovery of RNA proximal proteins via proximity-dependent biotinylation.

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  7 in total

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