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Identification of Non-Canonical Translation Products in C. elegans Using Tandem Mass Spectrometry.


ABSTRACT: Transcriptome and ribosome sequencing have revealed the existence of many non-canonical transcripts, mainly containing splice variants, ncRNA, sORFs and altORFs. However, identification and characterization of products that may be translated out of these remains a challenge. Addressing this, we here report on 552 non-canonical proteins and splice variants in the model organism C. elegans using tandem mass spectrometry. Aided by sequencing-based prediction, we generated a custom proteome database tailored to search for non-canonical translation products of C. elegans. Using this database, we mined available mass spectrometric resources of C. elegans, from which 51 novel, non-canonical proteins could be identified. Furthermore, we utilized diverse proteomic and peptidomic strategies to detect 40 novel non-canonical proteins in C. elegans by LC-TIMS-MS/MS, of which 6 were common with our meta-analysis of existing resources. Together, this permits us to provide a resource with detailed annotation of 467 splice variants and 85 novel proteins mapped onto UTRs, non-coding regions and alternative open reading frames of the C. elegans genome.

SUBMITTER: Parmar BS 

PROVIDER: S-EPMC8575065 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

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Identification of Non-Canonical Translation Products in <i>C. elegans</i> Using Tandem Mass Spectrometry.

Parmar Bhavesh S BS   Peeters Marlies K R MKR   Boonen Kurt K   Clark Ellie C EC   Baggerman Geert G   Menschaert Gerben G   Temmerman Liesbet L  

Frontiers in genetics 20211025


Transcriptome and ribosome sequencing have revealed the existence of many non-canonical transcripts, mainly containing splice variants, ncRNA, sORFs and altORFs. However, identification and characterization of products that may be translated out of these remains a challenge. Addressing this, we here report on 552 non-canonical proteins and splice variants in the model organism <i>C. elegans</i> using tandem mass spectrometry<i>.</i> Aided by sequencing-based prediction, we generated a custom pro  ...[more]

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