Reduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development

PLoS Genet. 2019 Sep 16;15(9):e1008338. doi: 10.1371/journal.pgen.1008338. eCollection 2019 Sep.

Abstract

Animal development requires the execution of specific transcriptional programs in different sets of cells to build tissues and functional organs. Transcripts are exported from the nucleus to the cytoplasm where they are translated into proteins that, ultimately, carry out the cellular functions. Here we show that in Caenorhabditis elegans, reduction of mRNA export strongly affects epithelial morphogenesis and germline proliferation while other tissues remain relatively unaffected. Epithelialization and gamete formation demand a large number of transcripts in the cytoplasm for the duration of these processes. In addition, our findings highlight the existence of a regulatory feedback mechanism that activates gene expression in response to low levels of cytoplasmic mRNA. We expand the genetic characterization of nuclear export factor NXF-1 to other members of the mRNA export pathway to model mRNA export and recycling of NXF-1 back to the nucleus. Our model explains how mutations in genes involved in general processes, such as mRNA export, may result in tissue-specific developmental phenotypes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus / genetics
  • Amino Acid Sequence
  • Animals
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism
  • Cell Nucleus / genetics
  • Cytoplasm / metabolism
  • Nucleocytoplasmic Transport Proteins / genetics
  • Organ Specificity / genetics*
  • RNA Transport / genetics
  • RNA Transport / physiology*
  • RNA, Messenger / metabolism
  • RNA, Messenger / physiology*
  • RNA-Binding Proteins / genetics

Substances

  • Caenorhabditis elegans Proteins
  • Nucleocytoplasmic Transport Proteins
  • RNA, Messenger
  • RNA-Binding Proteins

Grants and funding

JC is funded by RiojaSalud Foundation, the Spanish Ministry of Science, Innovation and Universities (Grant: PGC2018-094276-B-I00), the European program RefbioII (Grants: Momeneu and Age-hdacis) and by a donation of Muebles Guerra, Haro, La Rioja, Spain. HK and HN were supported by a grant (no: 275911) from the South East Norway Regional Health Authority. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.