Evidence map›Paper›PMID 37288606›Full record

ArticleMolecular biology and evolution2023

Cytoplasmic Polyadenylation Is an Ancestral Hallmark of Early Development in Animals.

Labib Rouhana, Allison Edgar, Fredrik Hugosson, Valeria Dountcheva, Mark Q Martindale, Joseph F Ryan

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Poly(A) tail regulation in stem cells and early development.Cell regeneration (London, England) · 2025
    Review
  3. Article
  4. Role of CPEBs in Learning and Memory.Journal of neurochemistry · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Labib RouhanaDepartment of Biology, University of Massachusetts Boston, Boston, MA, USA.ORCID 0000-0002-2886-5095
Allison EdgarWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL, USA.
Fredrik HugossonWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL, USA.
Valeria DountchevaDepartment of Biology, University of Massachusetts Boston, Boston, MA, USA.
Mark Q MartindaleWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL, USA.
Joseph F RyanWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL, USA.ORCID 0000-0001-5478-0522
Whitney Museum of American Art · USUniversity of Massachusetts Boston · US

Funding

Discovery of germline genes and regulatory networks in planariansR15HD082754 · NICHD · WRIGHT STATE UNIVERSITY · PI ROUHANA, LABIB · 2014 to 2024
$1.3M
NICHD NIH HHS R15 HD082754
6 · The paper itself

Abstract

Differential regulation of gene expression has produced the astonishing diversity of life on Earth. Understanding the origin and evolution of mechanistic innovations for control of gene expression is therefore integral to evolutionary and developmental biology. Cytoplasmic polyadenylation is the biochemical extension of polyadenosine at the 3'-end of cytoplasmic mRNAs. This process regulates the translation of specific maternal transcripts and is mediated by the Cytoplasmic Polyadenylation Element-Binding Protein family (CPEBs). Genes that code for CPEBs are amongst a very few that are present in animals but missing in nonanimal lineages. Whether cytoplasmic polyadenylation is present in non-bilaterian animals (i.e., sponges, ctenophores, placozoans, and cnidarians) remains unknown. We have conducted phylogenetic analyses of CPEBs, and our results show that CPEB1 and CPEB2 subfamilies originated in the animal stem lineage. Our assessment of expression in the sea anemone, Nematostella vectensis (Cnidaria), and the comb jelly, Mnemiopsis leidyi (Ctenophora), demonstrates that maternal expression of CPEB1 and the catalytic subunit of the cytoplasmic polyadenylation machinery (GLD2) is an ancient feature that is conserved across animals. Furthermore, our measurements of poly(A)-tail elongation reveal that key targets of cytoplasmic polyadenylation are shared between vertebrates, cnidarians, and ctenophores, indicating that this mechanism orchestrates a regulatory network that is conserved throughout animal evolution. We postulate that cytoplasmic polyadenylation through CPEBs was a fundamental innovation that contributed to animal evolution from unicellular life.

Indexed as

CtenophoraSea AnemonesAnimalsPhylogenyPolyadenylationCnidariaCtenophoracytoplasmic polyadenylationevolutionpost-transcriptional regulation

Identifiers

PMID37288606
PMCPMC10284499
OpenAlexW4379768828

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.