Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.

The biology and behavior of adults differ substantially from those of developing animals, and cell-specific information is critical for deciphering the biology of multicellular animals. Thus, adult tissue-specific transcriptomic data are critical for understanding molecular mechanisms that control t...

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Main Authors: Rachel Kaletsky, Victoria Yao, April Williams, Alexi M Runnels, Alicja Tadych, Shiyi Zhou, Olga G Troyanskaya, Coleen T Murphy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-08-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC6105014?pdf=render
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spelling doaj-ef018f0f09e5443c86c14b693df8f4c42020-11-25T02:33:13ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042018-08-01148e100755910.1371/journal.pgen.1007559Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.Rachel KaletskyVictoria YaoApril WilliamsAlexi M RunnelsAlicja TadychShiyi ZhouOlga G TroyanskayaColeen T MurphyThe biology and behavior of adults differ substantially from those of developing animals, and cell-specific information is critical for deciphering the biology of multicellular animals. Thus, adult tissue-specific transcriptomic data are critical for understanding molecular mechanisms that control their phenotypes. We used adult cell-specific isolation to identify the transcriptomes of C. elegans' four major tissues (or "tissue-ome"), identifying ubiquitously expressed and tissue-specific "enriched" genes. These data newly reveal the hypodermis' metabolic character, suggest potential worm-human tissue orthologies, and identify tissue-specific changes in the Insulin/IGF-1 signaling pathway. Tissue-specific alternative splicing analysis identified a large set of collagen isoforms. Finally, we developed a machine learning-based prediction tool for 76 sub-tissue cell types, which we used to predict cellular expression differences in IIS/FOXO signaling, stage-specific TGF-β activity, and basal vs. memory-induced CREB transcription. Together, these data provide a rich resource for understanding the biology governing multicellular adult animals.http://europepmc.org/articles/PMC6105014?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rachel Kaletsky
Victoria Yao
April Williams
Alexi M Runnels
Alicja Tadych
Shiyi Zhou
Olga G Troyanskaya
Coleen T Murphy
spellingShingle Rachel Kaletsky
Victoria Yao
April Williams
Alexi M Runnels
Alicja Tadych
Shiyi Zhou
Olga G Troyanskaya
Coleen T Murphy
Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
PLoS Genetics
author_facet Rachel Kaletsky
Victoria Yao
April Williams
Alexi M Runnels
Alicja Tadych
Shiyi Zhou
Olga G Troyanskaya
Coleen T Murphy
author_sort Rachel Kaletsky
title Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
title_short Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
title_full Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
title_fullStr Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
title_full_unstemmed Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
title_sort transcriptome analysis of adult caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2018-08-01
description The biology and behavior of adults differ substantially from those of developing animals, and cell-specific information is critical for deciphering the biology of multicellular animals. Thus, adult tissue-specific transcriptomic data are critical for understanding molecular mechanisms that control their phenotypes. We used adult cell-specific isolation to identify the transcriptomes of C. elegans' four major tissues (or "tissue-ome"), identifying ubiquitously expressed and tissue-specific "enriched" genes. These data newly reveal the hypodermis' metabolic character, suggest potential worm-human tissue orthologies, and identify tissue-specific changes in the Insulin/IGF-1 signaling pathway. Tissue-specific alternative splicing analysis identified a large set of collagen isoforms. Finally, we developed a machine learning-based prediction tool for 76 sub-tissue cell types, which we used to predict cellular expression differences in IIS/FOXO signaling, stage-specific TGF-β activity, and basal vs. memory-induced CREB transcription. Together, these data provide a rich resource for understanding the biology governing multicellular adult animals.
url http://europepmc.org/articles/PMC6105014?pdf=render
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