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Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod

BACKGROUND: Zygotic transcription in fish embryos initiates around the time of gastrulation, and all prior development is initiated and controlled by maternally derived messenger RNAs. Atlantic cod egg and embryo viability is variable, and it is hypothesized that the early development depends upon t...

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Autores principales: Kleppe, Lene, Edvardsen, Rolf B, Kuhl, Heiner, Malde, Ketil, Furmanek, Tomasz, Drivenes, Øyvind, Reinhardt, Richard, Taranger, Geir L, Wargelius, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462720/
https://www.ncbi.nlm.nih.gov/pubmed/22937762
http://dx.doi.org/10.1186/1471-2164-13-443
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author Kleppe, Lene
Edvardsen, Rolf B
Kuhl, Heiner
Malde, Ketil
Furmanek, Tomasz
Drivenes, Øyvind
Reinhardt, Richard
Taranger, Geir L
Wargelius, Anna
author_facet Kleppe, Lene
Edvardsen, Rolf B
Kuhl, Heiner
Malde, Ketil
Furmanek, Tomasz
Drivenes, Øyvind
Reinhardt, Richard
Taranger, Geir L
Wargelius, Anna
author_sort Kleppe, Lene
collection PubMed
description BACKGROUND: Zygotic transcription in fish embryos initiates around the time of gastrulation, and all prior development is initiated and controlled by maternally derived messenger RNAs. Atlantic cod egg and embryo viability is variable, and it is hypothesized that the early development depends upon the feature of these maternal RNAs. Both the length and the presence of specific motifs in the 3’UTR of maternal RNAs are believed to regulate expression and stability of the maternal transcripts. Therefore, the aim of this study was to characterize the overall composition and 3’UTR structure of the most common maternal RNAs found in cod eggs and pre-zygotic embryos. RESULTS: 22229 Sanger-sequences were obtained from 3’-end sequenced cDNA libraries prepared from oocyte, 1-2 cell, blastula and gastrula stages. Quantitative PCR revealed that EST copy number below 9 did not reflect the gene expression profile. Consequently genes represented by less than 9 ESTs were excluded from downstream analyses, in addition to sequences with low-quality gene hits. This provided 12764 EST sequences, encoding 257 unique genes, for further analysis. Mitochondrial transcripts accounted for 45.9-50.6% of the transcripts isolated from the maternal stages, but only 12.2% of those present at the onset of zygotic transcription. 3’UTR length was predicted in nuclear sequences with poly-A tail, which identified 191 3’UTRs. Their characteristics indicated a more complex regulation of transcripts that are abundant prior to the onset of zygotic transcription. Maternal and stable transcripts had longer 3’UTR (mean 187.1 and 208.8 bp) and more 3’UTR isoforms (45.7 and 34.6%) compared to zygotic transcripts, where 15.4% had 3’UTR isoforms and the mean 3’UTR length was 76 bp. Also, diversity and the amount of putative polyadenylation motifs were higher in both maternal and stable transcripts. CONCLUSIONS: We report on the most pronounced processes in the maternally transferred cod transcriptome. Maternal stages are characterized by a rich abundance of mitochondrial transcripts. Maternal and stable transcripts display longer 3'UTRs with more variation of both polyadenylation motifs and 3'UTR isoforms. These data suggest that cod eggs possess a complex array of maternal RNAs which likely act to tightly regulate early developmental processes in the newly fertilized egg.
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spelling pubmed-34627202012-10-03 Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod Kleppe, Lene Edvardsen, Rolf B Kuhl, Heiner Malde, Ketil Furmanek, Tomasz Drivenes, Øyvind Reinhardt, Richard Taranger, Geir L Wargelius, Anna BMC Genomics Research Article BACKGROUND: Zygotic transcription in fish embryos initiates around the time of gastrulation, and all prior development is initiated and controlled by maternally derived messenger RNAs. Atlantic cod egg and embryo viability is variable, and it is hypothesized that the early development depends upon the feature of these maternal RNAs. Both the length and the presence of specific motifs in the 3’UTR of maternal RNAs are believed to regulate expression and stability of the maternal transcripts. Therefore, the aim of this study was to characterize the overall composition and 3’UTR structure of the most common maternal RNAs found in cod eggs and pre-zygotic embryos. RESULTS: 22229 Sanger-sequences were obtained from 3’-end sequenced cDNA libraries prepared from oocyte, 1-2 cell, blastula and gastrula stages. Quantitative PCR revealed that EST copy number below 9 did not reflect the gene expression profile. Consequently genes represented by less than 9 ESTs were excluded from downstream analyses, in addition to sequences with low-quality gene hits. This provided 12764 EST sequences, encoding 257 unique genes, for further analysis. Mitochondrial transcripts accounted for 45.9-50.6% of the transcripts isolated from the maternal stages, but only 12.2% of those present at the onset of zygotic transcription. 3’UTR length was predicted in nuclear sequences with poly-A tail, which identified 191 3’UTRs. Their characteristics indicated a more complex regulation of transcripts that are abundant prior to the onset of zygotic transcription. Maternal and stable transcripts had longer 3’UTR (mean 187.1 and 208.8 bp) and more 3’UTR isoforms (45.7 and 34.6%) compared to zygotic transcripts, where 15.4% had 3’UTR isoforms and the mean 3’UTR length was 76 bp. Also, diversity and the amount of putative polyadenylation motifs were higher in both maternal and stable transcripts. CONCLUSIONS: We report on the most pronounced processes in the maternally transferred cod transcriptome. Maternal stages are characterized by a rich abundance of mitochondrial transcripts. Maternal and stable transcripts display longer 3'UTRs with more variation of both polyadenylation motifs and 3'UTR isoforms. These data suggest that cod eggs possess a complex array of maternal RNAs which likely act to tightly regulate early developmental processes in the newly fertilized egg. BioMed Central 2012-09-01 /pmc/articles/PMC3462720/ /pubmed/22937762 http://dx.doi.org/10.1186/1471-2164-13-443 Text en Copyright ©2012 Kleppe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kleppe, Lene
Edvardsen, Rolf B
Kuhl, Heiner
Malde, Ketil
Furmanek, Tomasz
Drivenes, Øyvind
Reinhardt, Richard
Taranger, Geir L
Wargelius, Anna
Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod
title Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod
title_full Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod
title_fullStr Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod
title_full_unstemmed Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod
title_short Maternal 3’UTRs: from egg to onset of zygotic transcription in Atlantic cod
title_sort maternal 3’utrs: from egg to onset of zygotic transcription in atlantic cod
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462720/
https://www.ncbi.nlm.nih.gov/pubmed/22937762
http://dx.doi.org/10.1186/1471-2164-13-443
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