Evidence map›Paper›PMID 27975270›Full record

ReviewAdvances in experimental medicine and biology2017

Controlling the Messenger: Regulated Translation of Maternal mRNAs in Xenopus laevis Development.

Michael D Sheets, Catherine A Fox, Megan E Dowdle, Susanne Imboden Blaser, Andy Chung, Sookhee Park

Abstract readReview
In one paragraph

Review in Advances in experimental medicine and biology, 2017. 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
2.7field-weighted citation impact, top 9% 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, 18 citations in OpenAlex.

  1. Escaping Constraints to Innovate: Maternal Neofunctionalization in a HoxB4 Duplicate.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2026
    Article
  2. Article
  3. Article
  4. Bicaudal-C Post-transcriptional regulator of cell fates and functions.Frontiers in cell and developmental biology · 2022
    Review
  5. Review
  6. Article
  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 1 institution in 1 country.

Michael D SheetsDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin, 440 Henry Mall, Madison, WI, 53706, USA. mdsheets@wisc.edu.
Catherine A FoxDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin, 440 Henry Mall, Madison, WI, 53706, USA.
Megan E DowdleDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin, 440 Henry Mall, Madison, WI, 53706, USA.
Susanne Imboden BlaserDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin, 440 Henry Mall, Madison, WI, 53706, USA.
Andy ChungDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin, 440 Henry Mall, Madison, WI, 53706, USA.
Sookhee ParkDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin, 440 Henry Mall, Madison, WI, 53706, USA.
University of Wisconsin–Madison · US

Funding

BIOTECHNOLOGY TRAINING PROGRAMT32GM008349 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, BRIAN G · 1989 to 2019
$22.5M
Origin Recognition Complex at Transcriptional SilencersR01GM056890 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, CATHERINE A · 1998 to 2020
$6.4M
Enabling Xenopus oocytes and embryos to perform RNAiR21HD069345 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI SHEETS, MICHAEL D · 2012 to 2013
$402k
Defining the Xenopus translatomeR21HD076828 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI SHEETS, MICHAEL D · 2013 to 2014
$393k
NICHD NIH HHS R21 HD069345NICHD NIH HHS R21 HD076828NIGMS NIH HHS R01 GM056890NIGMS NIH HHS T32 GM008349
6 · The paper itself

Abstract

The selective translation of maternal mRNAs encoding cell-fate determinants drives the earliest decisions of embryogenesis that establish the vertebrate body plan. This chapter will discuss studies in Xenopus laevis that provide insights into mechanisms underlying this translational control. Xenopus has been a powerful model organism for many discoveries relevant to the translational control of maternal mRNAs because of the large size of its oocytes and eggs that allow for microinjection of molecules and the relative ease of manipulating the oocyte to egg transition (maturation) and fertilization in culture. Consequently, many key studies have focused on the expression of maternal mRNAs during the oocyte to egg transition (the meiotic cell cycle) and the rapid cell divisions immediately following fertilization. This research has made seminal contributions to our understanding of translational regulatory mechanisms, but while some of the mRNAs under consideration at these stages encode cell-fate determinants, many encode cell cycle regulatory proteins that drive these early cell cycles. In contrast, while maternal mRNAs encoding key developmental (i.e., cell-fate) regulators that function after the first cleavage stages may exploit aspects of these foundational mechanisms, studies reveal that these mRNAs must also rely on distinct and, as of yet, incompletely understood mechanisms. These findings are logical because the functions of such developmental regulatory proteins have requirements distinct from cell cycle regulators, including becoming relevant only after fertilization and then only in specific cells of the embryo. Indeed, key maternal cell-fate determinants must be made available in exquisitely precise amounts (usually low), only at specific times and in specific cells during embryogenesis. To provide an appreciation for the regulation of maternal cell-fate determinant expression, an overview of the maternal phase of Xenopus embryogenesis will be presented. This section will be followed by a review of translational mechanisms operating in oocytes, eggs, and early cleavage-stage embryos and conclude with a discussion of how the regulation of key maternal cell-fate determinants at the level of translation functions in Xenopus embryogenesis. A key theme is that the molecular asymmetries critical for forming the body axes are established and further elaborated upon by the selective temporal and spatial regulation of maternal mRNA translation.

Indexed as

Protein BiosynthesisAnimalsCell CycleEmbryonic DevelopmentFemaleGene Expression Regulation, DevelopmentalOocytesRNA, MessengerTranscription, GeneticXenopus laevisRNA, MessengerEmbryonic asymmetryMaternal mRNARegulated translationXenopus

Identifiers

PMID27975270
PMCPMC5652302
OpenAlexW2566879086

What OpenQuestion holds

Textmetadata
LicenceTDM
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.