Gene duplication and transposition of mobile elements drive evolution of the Rpv3 resistance locus in grapevine. (11th November 2019)
- Record Type:
- Journal Article
- Title:
- Gene duplication and transposition of mobile elements drive evolution of the Rpv3 resistance locus in grapevine. (11th November 2019)
- Main Title:
- Gene duplication and transposition of mobile elements drive evolution of the Rpv3 resistance locus in grapevine
- Authors:
- Foria, Serena
Copetti, Dario
Eisenmann, Birgit
Magris, Gabriele
Vidotto, Michele
Scalabrin, Simone
Testolin, Raffaele
Cipriani, Guido
Wiedemann‐Merdinoglu, Sabine
Bogs, Jochen
Di Gaspero, Gabriele
Morgante, Michele - Abstract:
- Summary: A wild grape haplotype (Rpv3‐1) confers resistance to Plasmopara viticola . We mapped the causal factor for resistance to an interval containing a TIR‐NB‐LRR ( TNL ) gene pair that originated 1.6–2.6 million years ago by a tandem segmental duplication. Transient coexpression of the TNL pair in Vitis vinifera leaves activated pathogen‐induced necrosis and reduced sporulation compared with control leaves. Even though transcripts of the TNL pair from the wild haplotype appear to be partially subject to nonsense‐mediated mRNA decay, mature mRNA levels in a homozygous resistant genotype were individually higher than the mRNA trace levels observed for the orthologous single‐copy TNL in sensitive genotypes. Allelic expression imbalance in a resistant heterozygote confirmed that cis ‐acting regulatory variation promotes expression in the wild haplotype. The movement of transposable elements had a major impact on the generation of haplotype diversity, altering the DNA context around similar TNL coding sequences and the GC‐content in their proximal 5′‐intergenic regions. The wild and domesticated haplotypes also diverged in conserved single‐copy intergenic DNA, but the highest divergence was observed in intraspecific and not in interspecific comparisons. In this case, introgression breeding did not transgress the genetic boundaries of the domesticated species, because haplotypes present in modern varieties sometimes predate speciation events between wild and cultivatedSummary: A wild grape haplotype (Rpv3‐1) confers resistance to Plasmopara viticola . We mapped the causal factor for resistance to an interval containing a TIR‐NB‐LRR ( TNL ) gene pair that originated 1.6–2.6 million years ago by a tandem segmental duplication. Transient coexpression of the TNL pair in Vitis vinifera leaves activated pathogen‐induced necrosis and reduced sporulation compared with control leaves. Even though transcripts of the TNL pair from the wild haplotype appear to be partially subject to nonsense‐mediated mRNA decay, mature mRNA levels in a homozygous resistant genotype were individually higher than the mRNA trace levels observed for the orthologous single‐copy TNL in sensitive genotypes. Allelic expression imbalance in a resistant heterozygote confirmed that cis ‐acting regulatory variation promotes expression in the wild haplotype. The movement of transposable elements had a major impact on the generation of haplotype diversity, altering the DNA context around similar TNL coding sequences and the GC‐content in their proximal 5′‐intergenic regions. The wild and domesticated haplotypes also diverged in conserved single‐copy intergenic DNA, but the highest divergence was observed in intraspecific and not in interspecific comparisons. In this case, introgression breeding did not transgress the genetic boundaries of the domesticated species, because haplotypes present in modern varieties sometimes predate speciation events between wild and cultivated species. Significance Statement: The causal factor for Plasmopara viticola ‐induced necrosis was identified by positional cloning within a wild grape haplotype that showed high structural variation but limited nucleotide divergence compared with haplotypes retained in the domesticated species. We report here on the molecular events that led to the stepwise evolution of the Rpv3 haplotype that has had a major role in grapevine breeding for downy mildew resistance. … (more)
- Is Part Of:
- Plant journal. Volume 101:Number 3(2020)
- Journal:
- Plant journal
- Issue:
- Volume 101:Number 3(2020)
- Issue Display:
- Volume 101, Issue 3 (2020)
- Year:
- 2020
- Volume:
- 101
- Issue:
- 3
- Issue Sort Value:
- 2020-0101-0003-0000
- Page Start:
- 529
- Page End:
- 542
- Publication Date:
- 2019-11-11
- Subjects:
- Vitis vinifera -- introgression breeding -- disease resistance -- grapevine -- tandem gene duplicates
Plant molecular biology -- Periodicals
Plant cells and tissues -- Periodicals
Botany -- Periodicals
580 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-313X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/tpj.14551 ↗
- Languages:
- English
- ISSNs:
- 0960-7412
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6519.200000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17055.xml