2015
DOI: 10.1186/s12864-015-1901-x
|View full text |Cite
|
Sign up to set email alerts
|

Identification of novel small ncRNAs in pollen of tomato

Abstract: BackgroundThe unprecedented role of sncRNAs in the regulation of pollen biogenesis on both transcriptional and epigenetic levels has been experimentally proven. However, little is known about their global regulation, especially under stress conditions. We used tomato pollen in order to identify pollen stage-specific sncRNAs and their target mRNAs. We further deployed elevated temperatures to discern stress responsive sncRNAs. For this purpose high throughput sncRNA-sequencing as well as Massive Analysis of cDN… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
25
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
5
4

Relationship

2
7

Authors

Journals

citations
Cited by 28 publications
(25 citation statements)
references
References 115 publications
(115 reference statements)
0
25
0
Order By: Relevance
“…RNA was extracted by miRVana small RNA extraction kit (Ambion Life technologies, Carlsbad, California, USA), from caryopses harvested 8 days after anthesis. After quality control (Bioanalyzer, Agilent, Santa Clara, California, USA), small RNA libraries (two biological replicates for each condition) were processed as described in [52] for sncRNA libraries with TrueQuant technology for elimination of PCR bias. The fraction of 140-160 bp was size-selected by preparative polyacrylamide gel electrophoresis for Illumina HiSeq2000 sequencing of the small RNA fraction of 17-40 bp including the miRNA.…”
Section: Small Rna Sequencingmentioning
confidence: 99%
“…RNA was extracted by miRVana small RNA extraction kit (Ambion Life technologies, Carlsbad, California, USA), from caryopses harvested 8 days after anthesis. After quality control (Bioanalyzer, Agilent, Santa Clara, California, USA), small RNA libraries (two biological replicates for each condition) were processed as described in [52] for sncRNA libraries with TrueQuant technology for elimination of PCR bias. The fraction of 140-160 bp was size-selected by preparative polyacrylamide gel electrophoresis for Illumina HiSeq2000 sequencing of the small RNA fraction of 17-40 bp including the miRNA.…”
Section: Small Rna Sequencingmentioning
confidence: 99%
“…However, the miRNAs involved in this process in tomato plants remain poorly understood. Only four differentially expressed novel miRNAs have been identified from the pollen of tomato plants upon 38 °C treatment for 1 h [ 30 ]. No study has been performed to identify the heat-responsive miRNAs in stamens and pistils of tomato plants.…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, gene expression studies by RNA-seq permitted to identify around 150 different pollen-expressed genes in different plant species associated with a range of different functions, including cell wall metabolism, cytoskeleton and signaling (Honys and Twell 2003;Palanivelu and Tsukamoto 2012;Rutley and Twell 2015). Moreover, RNA-seq also shed light on the composition and expression profile of pollen small RNAs (Bokszczanin et al 2015;Borges et al 2011;GrantDownton et al 2009;Li et al 2013;Lu et al 2015;Slotkin et al 2009;Zhang et al 2009). …”
Section: Next Generation Sequencing (Ngs) Datamentioning
confidence: 96%
“…In Bokszczanin et al (2015), novel small nuclear RNAs (sncRNAs) from tomato tetrads, post-meiotic and mature pollen, expressed under control or heat stress conditions were detected. A specific reference Web site that describes this collection is available at http://www.cab.unina.it/mirna-pollen.…”
Section: Next Generation Sequencing (Ngs) Datamentioning
confidence: 98%