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Portrait of an oocyte: our obscure origin
Roger Gosden, Bora Lee
Roger Gosden, Bora Lee
Published April 1, 2010
Citation Information: J Clin Invest. 2010;120(4):973-983. https://doi.org/10.1172/JCI41294.
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Portrait of an oocyte: our obscure origin

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Abstract

Oocytes play a pivotal role in the cycle of human life. As we discuss here, after emerging from germline stem cells in the fetus, they grow in a follicular niche in which development is harmonized for timely ovulation and hormone secretion after puberty. Most human oocytes have poor developmental competence and are peculiarly vulnerable to chromosomal malsegregation, especially as women pass the optimal years of fertility and may begin to turn to assisted reproductive technologies (ARTs) and egg donation. Research needs to focus on the molecular factors involved and the environmental niche required for optimal development of oocytes, with the aim of increasing their numbers and quality for ARTs, since these are the factors that so often limit human fertility.

Authors

Roger Gosden, Bora Lee

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Figure 4

Diagrammatic representation of the suppression of mRNA translation in RNP complexes in oocytes.

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Diagrammatic representation of the suppression of mRNA translation in RN...
After the freshly transcribed and spliced transcript is incorporated into a RNP complex, it can either be translated directly or enter a prolonged period of translational dormancy. Transcripts that can be stored contain a CPE at the 3′-untranslated end, to which the protein CPEB binds. Phosphorylation of the latter causes release of PARN from the complex, enabling GLD2 to elongate the poly(A) and hence facilitate translation by interaction with other proteins. In dormant mRNAs, another CPEB-associated protein, maskin, inhibits an initiation factor (eIF4G) required for recruiting the 40S ribosomal subunit to the 5′ end of the mRNA by binding the cap-binding eukaryotic initiation factor (4E). 40S, 40S ribosomal subunit.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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