The 5′-Untranslated Region of the ntp303 Gene Strongly Enhances Translation during Pollen Tube Growth, but Not during Pollen Maturation

Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the un...

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Published inPlant physiology (Bethesda) Vol. 129; no. 1; pp. 342 - 353
Main Authors Raymond J. M. Hulzink, Peter F. M. de Groot, Anton F. Croes, William Quaedvlieg, Dave Twell, Wullems, George J., Marinus M. A. van Herpen
Format Journal Article
LanguageEnglish
Published Rockville, MD American Society of Plant Biologists 01.05.2002
American Society of Plant Physiologists
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RNA
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Abstract Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp303 5′-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5′-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. The ntp303 5′-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3′-UTR sequences. Furthermore, enhanced luciferase activity directed by the ntp303 5′-UTR occurred predominantly at the post-transcriptional level. A series of 5′-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A $(\text{GAA})_{8}$ repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
AbstractList Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp303 5'-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5'-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. The ntp303 5'-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3'-UTR sequences. Furthermore, enhanced luciferase activity directed by the ntp303 5'-UTR occurred predominantly at the post-transcriptional level. A series of 5'-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A (GAA)(8) repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp303 5′-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5′-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. The ntp303 5′-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3′-UTR sequences. Furthermore, enhanced luciferase activity directed by the ntp303 5′-UTR occurred predominantly at the post-transcriptional level. A series of 5′-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A $(\text{GAA})_{8}$ repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp303 5′-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5′-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. The ntp303 5′-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3′-UTR sequences. Furthermore, enhanced luciferase activity directed by the ntp303 5′-UTR occurred predominantly at the post-transcriptional level. A series of 5′-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A (GAA) 8 repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp303 5'-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5'-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. The ntp303 5'-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3'-UTR sequences. Furthermore, enhanced luciferase activity directed by the ntp303 5'-UTR occurred predominantly at the post-transcriptional level. A series of 5'-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A (GAA) sub(8) repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
Abstract Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp3035′-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5′-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. Thentp303 5′-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3′-UTR sequences. Furthermore, enhanced luciferase activity directed by thentp303 5′-UTR occurred predominantly at the post-transcriptional level. A series of 5′-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A (GAA)8repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
Author Anton F. Croes
William Quaedvlieg
Wullems, George J.
Peter F. M. de Groot
Raymond J. M. Hulzink
Dave Twell
Marinus M. A. van Herpen
AuthorAffiliation Department of Experimental Botany, Plant Genetics, Catholic University Nijmegen, Toernooiveld 1, 6525 ED, Nijmegen, The Netherlands (R.J.M.H., P.F.M.d.G., A.F.C., W.Q., G.J.W., M.M.A.v.H.); and Department of Biology, University of Leicester, University Road, Leicester, LE17RH, United Kingdom (D.T.)
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Issue 1
Keywords 5' terminal-Sequence
Stability
Molecular structure
Growth
Activation
Nicotiana tabacum
Genetic translation
Pollen tube
Regulation(control)
Messenger RNA
Gene
Dicotyledones
Angiospermae
Regulatory sequence
Spermatophyta
Pollen
Property structure relationship
Solanaceae
Experimental plant
Language English
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Corresponding author; e-mail marinush@sci.kun.nl; fax 31–0–24–3553450.
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PublicationTitle Plant physiology (Bethesda)
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American Society of Plant Physiologists
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SSID ssj0001314
Score 1.9523985
Snippet Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen...
Abstract Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after...
Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen...
SourceID pubmedcentral
proquest
crossref
pubmed
pascalfrancis
jstor
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 342
SubjectTerms 3' Untranslated Regions - genetics
5' Untranslated Regions - chemistry
5' Untranslated Regions - genetics
Agronomy. Soil science and plant productions
Base Sequence
Biological and medical sciences
Development and Hormone Action
Developmental biology
Economic plant physiology
Flowering, floral biology, reproduction patterns
Fundamental and applied biological sciences. Psychology
Gene Deletion
Gene Expression Profiling
Gene expression regulation
Gene Expression Regulation, Plant
Gene fusion
Growth and development
luciferase
Luciferases - genetics
Luciferases - metabolism
Messenger RNA
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
ntp303 gene
Nucleic Acid Conformation
Plant physiology and development
Plant Proteins - genetics
Plants
Pollen
Pollen - growth & development
Pollen tubes
Promoter regions
Protein Biosynthesis - genetics
Recombinant Fusion Proteins - genetics
Recombinant Fusion Proteins - metabolism
Reproduction - genetics
RNA
RNA Processing, Post-Transcriptional
RNA, Messenger - genetics
RNA, Messenger - metabolism
Sexual reproduction
Translation. Translation factors. Protein processing
Untranslated regions
Vegetative and sexual reproduction, floral biology, fructification
Title The 5′-Untranslated Region of the ntp303 Gene Strongly Enhances Translation during Pollen Tube Growth, but Not during Pollen Maturation
URI https://www.jstor.org/stable/4280465
https://www.ncbi.nlm.nih.gov/pubmed/12011364
https://www.proquest.com/docview/218645391
https://search.proquest.com/docview/18306109
https://search.proquest.com/docview/71687680
https://pubmed.ncbi.nlm.nih.gov/PMC155897
Volume 129
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