Literature DB >> 27975270

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

Michael D Sheets1, Catherine A Fox2, Megan E Dowdle2, Susanne Imboden Blaser2, Andy Chung2, Sookhee Park2.   

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.

Entities:  

Keywords:  Embryonic asymmetry; Maternal mRNA; Regulated translation; Xenopus

Mesh:

Substances:

Year:  2017        PMID: 27975270      PMCID: PMC5652302          DOI: 10.1007/978-3-319-46095-6_2

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  157 in total

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Journal:  Cell       Date:  1996-05-17       Impact factor: 41.582

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Journal:  Dev Biol       Date:  1999-10-15       Impact factor: 3.582

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Journal:  Genes Dev       Date:  1995-12-01       Impact factor: 11.361

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Journal:  Development       Date:  2001-08       Impact factor: 6.868

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Journal:  Development       Date:  1996-12       Impact factor: 6.868

10.  Requirement of mouse BCCIP for neural development and progenitor proliferation.

Authors:  Yi-Yuan Huang; Huimei Lu; Stephany Liu; Roberto Droz-Rosario; Zhiyuan Shen
Journal:  PLoS One       Date:  2012-01-24       Impact factor: 3.240

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Authors:  Kevin Drew; Chanjae Lee; Rachael M Cox; Vy Dang; Caitlin C Devitt; Claire D McWhite; Ophelia Papoulas; Ryan L Huizar; Edward M Marcotte; John B Wallingford
Journal:  Dev Biol       Date:  2020-09-06       Impact factor: 3.582

Review 2.  Evolution and new frontiers of histology in bio-medical research.

Authors:  Maria Mazzarini; Mario Falchi; Daniele Bani; Anna Rita Migliaccio
Journal:  Microsc Res Tech       Date:  2020-09-11       Impact factor: 2.769

3.  YTH-RNA-binding protein prevents deleterious expression of meiotic proteins by tethering their mRNAs to nuclear foci.

Authors:  Yuichi Shichino; Yoko Otsubo; Yoshitaka Kimori; Masayuki Yamamoto; Akira Yamashita
Journal:  Elife       Date:  2018-02-09       Impact factor: 8.140

Review 4.  Bicaudal-C Post-transcriptional regulator of cell fates and functions.

Authors:  Megan E Dowdle; Charlotte R Kanzler; Cole R K Harder; Samuel Moffet; Maya N Walker; Michael D Sheets
Journal:  Front Cell Dev Biol       Date:  2022-09-07
  4 in total

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