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Vertebrate Development

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Attention for Chapter 2: Controlling the Messenger: Regulated Translation of Maternal mRNAs in Xenopus laevis Development.
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Chapter title
Controlling the Messenger: Regulated Translation of Maternal mRNAs in Xenopus laevis Development.
Chapter number 2
Book title
Vertebrate Development
Published in
Advances in experimental medicine and biology, December 2016
DOI 10.1007/978-3-319-46095-6_2
Pubmed ID
Book ISBNs
978-3-31-946093-2, 978-3-31-946095-6
Authors

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

Editors

Francisco Pelegri, Michael Danilchik, Ann Sutherland

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.

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The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 40 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 10%
Student > Doctoral Student 3 8%
Student > Ph. D. Student 3 8%
Other 2 5%
Student > Bachelor 2 5%
Other 3 8%
Unknown 23 57%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 10 25%
Nursing and Health Professions 2 5%
Agricultural and Biological Sciences 2 5%
Arts and Humanities 1 3%
Psychology 1 3%
Other 2 5%
Unknown 22 55%