Transcriptional analysis of a delayed-flowering mutant under short-day conditions reveal genes related to photoperiodic response in tossa jute (Corchorus olitorius L.)

•A gamma-irradiated mutant of jute, pfr 59 exhibited significantly delayed flowering-time phenotype in comparison to its wild-type plant JRO204.•Transcriptome from shoot apices of mutant and wild-type plant produced a merged assembly of 14050 transcripts with more than 90% aligning to the published...

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Published in:Industrial crops and products Vol. 132; pp. 476 - 486
Main Authors: Choudhary, Shashi Bhushan, Saha, Dipnarayan, Sharma, Hariom Kumar, Chowdhury, Isholeena, Kumar, A. Anil, Jambhulkar, Sanjay Kumar, Mitra, Jivan
Format: Journal Article
Language:English
Published: Elsevier B.V 01-06-2019
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Abstract •A gamma-irradiated mutant of jute, pfr 59 exhibited significantly delayed flowering-time phenotype in comparison to its wild-type plant JRO204.•Transcriptome from shoot apices of mutant and wild-type plant produced a merged assembly of 14050 transcripts with more than 90% aligning to the published jute genomes.•Digital gene expression analysis revealed 240 differentially expressed transcripts of which 10 transcripts showed homology to known photoperiodic genes of Arabidopsis.•Differential expression pattern of nine putative photoperiodic transcripts in leaf and shoot apex of mutant and wild-type infers their role in flowering-time regulation in jute. Photoperiod profoundly determines reproductive and vegetative development in jute which is extremely correlated to fibre yield and quality. Yet, our understanding of how the photoperiodic genes regulate vegetative and reproductive growth in jute remain unresolved. We developed RNA-seq data from shoot apex tissues of a delayed-flowering mutant (pfr 59) and its wild-type cultivar JRO-204 grown under short-day conditions. A merged de novo transcriptome assembly of 14,050 high-quality transcripts with N50 length of 1371 base-pairs, was constructed from the filtered RNA-seq data. Digital gene expression analysis produced 240 differentially expressed transcripts (DETs) between pfr 59 and JRO-204 shoot-apex transcriptome. Comparative analysis of these DETs showed homology to 75% and 42.5% sequences from the NCBI-NR and SWISSPROT databases, respectively. We could successfully align > 93% of the 14,050 merged transcripts and >65% of the 240 DETs to the three published jute genomes with >94.8% identity. Homology search for proteins from the FLOR-ID database led to the identification of 55 transcripts (3.9%) from the transcriptome assembly and 10 transcripts (4.2) from the DETs matching to photoperiod-related proteins. Gene expression validations of nine putative photoperiod-related DETs showed their differential expression patterns in leaf and shoot apex tissues of pfr 59 and JRO-204 under short-day conditions. The present report describes an assembly of a shoot apex transcriptome and identification of photoperiod-responsive transcripts with their putative role in regulating flowering mechanism in jute under short-day conditions. This crucial information may lay a foundation to devise genetic improvement strategies, such as gene-editing, for delaying the early onset of short-day flowering.
AbstractList •A gamma-irradiated mutant of jute, pfr 59 exhibited significantly delayed flowering-time phenotype in comparison to its wild-type plant JRO204.•Transcriptome from shoot apices of mutant and wild-type plant produced a merged assembly of 14050 transcripts with more than 90% aligning to the published jute genomes.•Digital gene expression analysis revealed 240 differentially expressed transcripts of which 10 transcripts showed homology to known photoperiodic genes of Arabidopsis.•Differential expression pattern of nine putative photoperiodic transcripts in leaf and shoot apex of mutant and wild-type infers their role in flowering-time regulation in jute. Photoperiod profoundly determines reproductive and vegetative development in jute which is extremely correlated to fibre yield and quality. Yet, our understanding of how the photoperiodic genes regulate vegetative and reproductive growth in jute remain unresolved. We developed RNA-seq data from shoot apex tissues of a delayed-flowering mutant (pfr 59) and its wild-type cultivar JRO-204 grown under short-day conditions. A merged de novo transcriptome assembly of 14,050 high-quality transcripts with N50 length of 1371 base-pairs, was constructed from the filtered RNA-seq data. Digital gene expression analysis produced 240 differentially expressed transcripts (DETs) between pfr 59 and JRO-204 shoot-apex transcriptome. Comparative analysis of these DETs showed homology to 75% and 42.5% sequences from the NCBI-NR and SWISSPROT databases, respectively. We could successfully align > 93% of the 14,050 merged transcripts and >65% of the 240 DETs to the three published jute genomes with >94.8% identity. Homology search for proteins from the FLOR-ID database led to the identification of 55 transcripts (3.9%) from the transcriptome assembly and 10 transcripts (4.2) from the DETs matching to photoperiod-related proteins. Gene expression validations of nine putative photoperiod-related DETs showed their differential expression patterns in leaf and shoot apex tissues of pfr 59 and JRO-204 under short-day conditions. The present report describes an assembly of a shoot apex transcriptome and identification of photoperiod-responsive transcripts with their putative role in regulating flowering mechanism in jute under short-day conditions. This crucial information may lay a foundation to devise genetic improvement strategies, such as gene-editing, for delaying the early onset of short-day flowering.
Author Kumar, A. Anil
Jambhulkar, Sanjay Kumar
Mitra, Jivan
Sharma, Hariom Kumar
Choudhary, Shashi Bhushan
Saha, Dipnarayan
Chowdhury, Isholeena
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  organization: Division of Crop Improvement, Indian Council of Agricultural Research-Central Research Institute for Jute and Allied Fibers, Barrackpore, Kolkata, West Bengal, 700 121, India
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  surname: Saha
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  organization: Division of Crop Improvement, Indian Council of Agricultural Research-Central Research Institute for Jute and Allied Fibers, Barrackpore, Kolkata, West Bengal, 700 121, India
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  givenname: Hariom Kumar
  orcidid: 0000-0002-7415-5289
  surname: Sharma
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  organization: Division of Crop Improvement, Indian Council of Agricultural Research-Central Research Institute for Jute and Allied Fibers, Barrackpore, Kolkata, West Bengal, 700 121, India
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  givenname: Isholeena
  surname: Chowdhury
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  organization: Division of Crop Improvement, Indian Council of Agricultural Research-Central Research Institute for Jute and Allied Fibers, Barrackpore, Kolkata, West Bengal, 700 121, India
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  givenname: A. Anil
  orcidid: 0000-0001-8855-7783
  surname: Kumar
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  givenname: Sanjay Kumar
  surname: Jambhulkar
  fullname: Jambhulkar, Sanjay Kumar
  organization: Nuclear Agriculture and Biotechnology Division, Bhabha Atomic Research Centre, 400085, Mumbai, India
– sequence: 7
  givenname: Jivan
  surname: Mitra
  fullname: Mitra, Jivan
  organization: Division of Crop Improvement, Indian Council of Agricultural Research-Central Research Institute for Jute and Allied Fibers, Barrackpore, Kolkata, West Bengal, 700 121, India
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CitedBy_id crossref_primary_10_1016_j_indcrop_2021_113913
crossref_primary_10_1007_s11032_023_01435_8
crossref_primary_10_1016_j_plaphy_2021_01_043
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Keywords nr
Short-day flowering
EST
Corchorus species
SD
QC
Bast fibre
EFS
min
s
RNA-seq
Shoot-apex transcriptome assembly
DAS
Delayed-flowering mutant
LD
NCBI
cDNA
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Photoperiodic genes
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Jute
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Snippet •A gamma-irradiated mutant of jute, pfr 59 exhibited significantly delayed flowering-time phenotype in comparison to its wild-type plant JRO204.•Transcriptome...
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SubjectTerms Bast fibre
Corchorus species
Delayed-flowering mutant
Jute
Photoperiodic genes
RNA-seq
Shoot-apex transcriptome assembly
Short-day flowering
Title Transcriptional analysis of a delayed-flowering mutant under short-day conditions reveal genes related to photoperiodic response in tossa jute (Corchorus olitorius L.)
URI https://dx.doi.org/10.1016/j.indcrop.2019.03.001
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