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Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs
Maternal mRNAs synthesized during oogenesis initiate the development of future generations. Some maternal mRNAs are either somatic or germline determinants and must be translationally repressed until embryogenesis. However, the translational repressors themselves are temporally regulated. We used po...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328254/ https://www.ncbi.nlm.nih.gov/pubmed/30590052 http://dx.doi.org/10.1016/j.celrep.2018.12.007 |
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author | Flora, Pooja Wong-Deyrup, Siu Wah Martin, Elliot Todd Palumbo, Ryan J. Nasrallah, Mohamad Oligney, Andrew Blatt, Patrick Patel, Dhruv Fuchs, Gabriele Rangan, Prashanth |
author_facet | Flora, Pooja Wong-Deyrup, Siu Wah Martin, Elliot Todd Palumbo, Ryan J. Nasrallah, Mohamad Oligney, Andrew Blatt, Patrick Patel, Dhruv Fuchs, Gabriele Rangan, Prashanth |
author_sort | Flora, Pooja |
collection | PubMed |
description | Maternal mRNAs synthesized during oogenesis initiate the development of future generations. Some maternal mRNAs are either somatic or germline determinants and must be translationally repressed until embryogenesis. However, the translational repressors themselves are temporally regulated. We used polar granule component (pgc), a Drosophila maternal mRNA, to ask how maternal transcripts are repressed while the regulatory landscape is shifting. pgc, a germline determinant, is translationally regulated throughout oogenesis. We find that different conserved RNA-binding proteins bind a 10-nt sequence in the 3′ UTR of pgc mRNA to continuously repress translation at different stages of oogenesis. Pumilio binds to this sequence in undifferentiated and early-differentiating oocytes to block Pgc translation. After differentiation, Bruno levels increase, allowing Bruno to bind the same sequence and take over translational repression of pgc mRNA. We have identified a class of maternal mRNAs that are regulated similarly, including zelda, the activator of the zygotic genome. |
format | Online Article Text |
id | pubmed-6328254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-63282542019-01-10 Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs Flora, Pooja Wong-Deyrup, Siu Wah Martin, Elliot Todd Palumbo, Ryan J. Nasrallah, Mohamad Oligney, Andrew Blatt, Patrick Patel, Dhruv Fuchs, Gabriele Rangan, Prashanth Cell Rep Article Maternal mRNAs synthesized during oogenesis initiate the development of future generations. Some maternal mRNAs are either somatic or germline determinants and must be translationally repressed until embryogenesis. However, the translational repressors themselves are temporally regulated. We used polar granule component (pgc), a Drosophila maternal mRNA, to ask how maternal transcripts are repressed while the regulatory landscape is shifting. pgc, a germline determinant, is translationally regulated throughout oogenesis. We find that different conserved RNA-binding proteins bind a 10-nt sequence in the 3′ UTR of pgc mRNA to continuously repress translation at different stages of oogenesis. Pumilio binds to this sequence in undifferentiated and early-differentiating oocytes to block Pgc translation. After differentiation, Bruno levels increase, allowing Bruno to bind the same sequence and take over translational repression of pgc mRNA. We have identified a class of maternal mRNAs that are regulated similarly, including zelda, the activator of the zygotic genome. 2018-12-26 /pmc/articles/PMC6328254/ /pubmed/30590052 http://dx.doi.org/10.1016/j.celrep.2018.12.007 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Flora, Pooja Wong-Deyrup, Siu Wah Martin, Elliot Todd Palumbo, Ryan J. Nasrallah, Mohamad Oligney, Andrew Blatt, Patrick Patel, Dhruv Fuchs, Gabriele Rangan, Prashanth Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs |
title | Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs |
title_full | Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs |
title_fullStr | Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs |
title_full_unstemmed | Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs |
title_short | Sequential Regulation of Maternal mRNAs through a Conserved cis-Acting Element in Their 3′ UTRs |
title_sort | sequential regulation of maternal mrnas through a conserved cis-acting element in their 3′ utrs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328254/ https://www.ncbi.nlm.nih.gov/pubmed/30590052 http://dx.doi.org/10.1016/j.celrep.2018.12.007 |
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