Asymmetric Transcript Discovery by RNA-seq in C. elegans Blastomeres Identifies neg-1, a Gene Important for Anterior Morphogenesis
- 1. University of North Carolina at Chapel Hill
- 2. University of Chicago
Description
After fertilization but prior to the onset of zygotic transcription, the C. elegans zygote cleaves asymmetrically to create the anterior AB and posterior P1 blastomeres, each of which goes on to generate distinct cell lineages. To understand how patterns of RNA inheritance and abundance arise after this first asymmetric cell division, we pooled hand-dissected AB and P1 blastomeres and performed RNA-seq. Our approach identified over 200 asymmetrically abundant mRNA transcripts. We confirmed symmetric or asymmetric abundance patterns for a subset of these transcripts using smFISH. smFISH also revealed heterogeneous subcellular patterning of the P1-enriched transcripts chs-1 and bpl-1. We screened transcripts enriched in a given blastomere for embryonic defects using RNAi. The gene neg-1 (F32D1.6) encoded an AB-enriched (anterior) transcript and was required for proper morphology of anterior tissues. In addition, analysis of the asymmetric transcripts yielded clues regarding the post-transcriptional mechanisms that control cellular mRNA abundance during asymmetric cell divisions, which are common in developing organisms.
Data availability
RNA-seq data associated with this paper are available at http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE59943 under the NCBI GEO identifier: GSE5994.Files
journal.pgen.1005117.pdf
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Additional details
Identifiers
- DOI
- 10.1371/journal.pgen.1005117
- Other
- oai:uchicago.tind.io:10802
Funding
- National Institutes of Health
- training grant
- Damon Runyon Cancer Research Foundation
- Postdoctoral Fellowship Award
- National Institutes of Health
- R01 GM083071
- National Science Foundation
- IOS 0917726
- University of North Carolina at Chapel Hill
- Summer Undergraduate Research Fellowship
- National Institutes of Health
- 5R01GM104050