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Integrated proteo-transcriptomic analyses reveal insights into regulation of pollen development stages and dynamics of cellular response to apple fruit crinkle viroid (AFCVd)-infection in Nicotiana tabacum
ID
Shrestha, Ankita
(
Author
),
ID
Kumar Mishra, Ajay
(
Author
),
ID
Matoušek, Jaroslav
(
Author
),
ID
Steinbachová, Lenka
(
Author
),
ID
Potěšil, David
(
Author
),
ID
Nath, Vishnu Sukumari
(
Author
),
ID
Awasthi, Praveen
(
Author
),
ID
Kocábek, Tomáš
(
Author
),
ID
Jakše, Jernej
(
Author
),
ID
Záveská Drábková, Lenka
(
Author
),
ID
Zdráhal, Zbyněk
(
Author
),
ID
Honys, David
(
Author
),
ID
Steger, Gerhard
(
Author
)
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MD5: 82480DA8D787DDF1F6B2CAFE5C5D253E
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https://www.mdpi.com/1422-0067/21/22/8700
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Abstract
Tobacco (Nicotiana tabacum) pollen is a well-suited model for studying many fundamental biological processes owing to its well-defined and distinct development stages. It is also one of the major agents involved in the transmission of infectious viroids, which is the primary mechanism of viroid pathogenicity in plants. However, some viroids are non-transmissible and may be possibly degraded or eliminated during the gradual process of pollen development maturation. The molecular details behind the response of developing pollen against the apple fruit crinkle viroid (AFCVd) infection and viroid eradication is largely unknown. In this study, we performed an integrative analysis of the transcriptome and proteome profiles to disentangle the molecular cascade of events governing the three pollen development stages: early bicellular pollen (stage 3, S3), late bicellular pollen (stage 5, S5), and 6 h-pollen tube (PT6). The integrated analysis delivered the molecular portraits of the developing pollen against AFCVd infection, including mechanistic insights into the viroid eradication during the last steps of pollen development. The isobaric tags for label-free relative quantification (iTRAQ) with digital gene expression (DGE) experiments led us to reliably identify subsets of 5321, 5286, and 6923 proteins and 64,033, 60,597, and 46,640 expressed genes in S3, S5, and PT6, respectively. In these subsets, 2234, 2108 proteins and 9207 and 14,065 mRNAs were differentially expressed in pairwise comparisons of three stages S5 vs. S3 and PT6 vs. S5 of control pollen in tobacco. Correlation analysis between the abundance of differentially expressed mRNAs (DEGs) and differentially expressed proteins (DEPs) in pairwise comparisons of three stages of pollen revealed numerous discordant changes in mRNA/protein pairs. Only a modest correlation was observed, indicative of divergent transcription, and its regulation and importance of post-transcriptional events in the determination of the fate of early and late pollen development in tobacco. The functional and enrichment analysis of correlated DEGs/DEPs revealed the activation in pathways involved in carbohydrate metabolism, amino acid metabolism, lipid metabolism, and cofactor as well as vitamin metabolism, which points to the importance of these metabolic pathways in pollen development. Furthermore, the detailed picture of AFCVd-infected correlated DEGs/DEPs was obtained in pairwise comparisons of three stages of infected pollen. The AFCVd infection caused the modulation of several genes involved in protein degradation, nuclear transport, phytohormone signaling, defense response, and phosphorylation. Intriguingly, we also identified several factors including, DNA-dependent RNA-polymerase, ribosomal protein, Argonaute (AGO) proteins, nucleotide binding proteins, and RNA exonucleases, which may plausibly involve in viroid stabilization and eradication during the last steps of pollen development. The present study provides essential insights into the transcriptional and translational dynamics of tobacco pollen, which further strengthens our understanding of plant-viroid interactions and support for future mechanistic studies directed at delineating the functional role of candidate factors involved in viroid elimination.
Language:
English
Keywords:
AFCVd propagation and eradication
,
viroid replication
,
viroid degradation
,
Nicotiana tabacum
,
male gametophyte
,
proteome
,
RNA sequencing
,
RT qPCR
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
BF - Biotechnical Faculty
Publication status:
Published
Publication version:
Version of Record
Year:
2020
Number of pages:
24 str.
Numbering:
Vol. 21, iss. 22, art. 8700
PID:
20.500.12556/RUL-134688
UDC:
577.2
ISSN on article:
1661-6596
DOI:
10.3390/ijms21228700
COBISS.SI-ID:
40325635
Publication date in RUL:
26.01.2022
Views:
856
Downloads:
132
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Record is a part of a journal
Title:
International journal of molecular sciences
Shortened title:
Int. j. mol. sci.
Publisher:
MDPI
ISSN:
1661-6596
COBISS.SI-ID:
36217605
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
18.11.2020
Secondary language
Language:
Slovenian
Keywords:
Nicotiana tabacum
,
tobak
,
pelod
,
bolezni rastlin
,
viroidi
,
proteomska analiza
,
transkriptomska analiza
,
RNA sekvenciranje
,
degradacija viroidov
Projects
Funder:
Other - Other funder or multiple funders
Funding programme:
Czech Science Foundation
Project number:
GACR 18-10515J
Funder:
Other - Other funder or multiple funders
Funding programme:
German Science Foundation
Project number:
DFG STE 465
Funder:
Other - Other funder or multiple funders
Funding programme:
Czech Science Foundation
Project number:
17-23183S
Funder:
Other - Other funder or multiple funders
Funding programme:
CR, Ministry of Education, Youth, and Sports
Project number:
CZ.02.1.01/0.0/0.0/16_019/0000738
Name:
Centre for Experimental Plant Biology
Funder:
EC - European Commission
Funding programme:
European Regional Development Fund
Name:
Centre for Experimental Plant Biology
Funder:
Other - Other funder or multiple funders
Funding programme:
CIISB
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