Haplotype-resolved genomes of geminivirus-resistant and geminivirus-susceptible African cassava cultivars.


Journal

BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720

Informations de publication

Date de publication:
18 09 2019
Historique:
received: 27 06 2019
accepted: 30 08 2019
entrez: 20 9 2019
pubmed: 20 9 2019
medline: 7 3 2020
Statut: epublish

Résumé

Cassava is an important food crop in tropical and sub-tropical regions worldwide. In Africa, cassava production is widely affected by cassava mosaic disease (CMD), which is caused by the African cassava mosaic geminivirus that is transmitted by whiteflies. Cassava breeders often use a single locus, CMD2, for introducing CMD resistance into susceptible cultivars. The CMD2 locus has been genetically mapped to a 10-Mbp region, but its organization and genes as well as their functions are unknown. We report haplotype-resolved de novo assemblies and annotations of the genomes for the African cassava cultivar TME (tropical Manihot esculenta), which is the origin of CMD2, and the CMD-susceptible cultivar 60444. The assemblies provide phased haplotype information for over 80% of the genomes. Haplotype comparison identified novel features previously hidden in collapsed and fragmented cassava genomes, including thousands of allelic variants, inter-haplotype diversity in coding regions, and patterns of diversification through allele-specific expression. Reconstruction of the CMD2 locus revealed a highly complex region with nearly identical gene sets but limited microsynteny between the two cultivars. The genome maps of the CMD2 locus in both 60444 and TME3, together with the newly annotated genes, will help the identification of the causal genetic basis of CMD2 resistance to geminiviruses. Our de novo cassava genome assemblies will also facilitate genetic mapping approaches to narrow the large CMD2 region to a few candidate genes for better informed strategies to develop robust geminivirus resistance in susceptible cassava cultivars.

Sections du résumé

BACKGROUND
Cassava is an important food crop in tropical and sub-tropical regions worldwide. In Africa, cassava production is widely affected by cassava mosaic disease (CMD), which is caused by the African cassava mosaic geminivirus that is transmitted by whiteflies. Cassava breeders often use a single locus, CMD2, for introducing CMD resistance into susceptible cultivars. The CMD2 locus has been genetically mapped to a 10-Mbp region, but its organization and genes as well as their functions are unknown.
RESULTS
We report haplotype-resolved de novo assemblies and annotations of the genomes for the African cassava cultivar TME (tropical Manihot esculenta), which is the origin of CMD2, and the CMD-susceptible cultivar 60444. The assemblies provide phased haplotype information for over 80% of the genomes. Haplotype comparison identified novel features previously hidden in collapsed and fragmented cassava genomes, including thousands of allelic variants, inter-haplotype diversity in coding regions, and patterns of diversification through allele-specific expression. Reconstruction of the CMD2 locus revealed a highly complex region with nearly identical gene sets but limited microsynteny between the two cultivars.
CONCLUSIONS
The genome maps of the CMD2 locus in both 60444 and TME3, together with the newly annotated genes, will help the identification of the causal genetic basis of CMD2 resistance to geminiviruses. Our de novo cassava genome assemblies will also facilitate genetic mapping approaches to narrow the large CMD2 region to a few candidate genes for better informed strategies to develop robust geminivirus resistance in susceptible cassava cultivars.

Identifiants

pubmed: 31533702
doi: 10.1186/s12915-019-0697-6
pii: 10.1186/s12915-019-0697-6
pmc: PMC6749633
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

75

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Auteurs

Joel-E Kuon (JE)

Department of Biology, Institute of Molecular Plant Biology, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland. joel-elias.kuon@biol.ethz.ch.

Weihong Qi (W)

Functional Genomics Center Zurich, Winterthurerstrasse 190, 8057, Zurich, Switzerland.

Pascal Schläpfer (P)

Department of Biology, Institute of Molecular Plant Biology, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland.

Matthias Hirsch-Hoffmann (M)

Department of Biology, Institute of Molecular Plant Biology, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland.

Philipp Rogalla von Bieberstein (PR)

Department of Biology, Institute of Molecular Plant Biology, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland.

Andrea Patrignani (A)

Functional Genomics Center Zurich, Winterthurerstrasse 190, 8057, Zurich, Switzerland.

Lucy Poveda (L)

Functional Genomics Center Zurich, Winterthurerstrasse 190, 8057, Zurich, Switzerland.

Stefan Grob (S)

Institute of Plant Biology, University of Zurich, Zollikerstrasse 107, 8008, Zurich, Switzerland.

Miyako Keller (M)

Department of Biology, Institute of Molecular Plant Biology, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland.

Rie Shimizu-Inatsugi (R)

Department of Evolutionary Biology and Environmental Studies, University of Zurich, Winterthurerstrasse 190, 8057, Zurich, Switzerland.

Ueli Grossniklaus (U)

Institute of Plant Biology, University of Zurich, Zollikerstrasse 107, 8008, Zurich, Switzerland.

Hervé Vanderschuren (H)

AgroBioChem Department, University of Liège, Passage des Déportés 2, Gembloux, Belgium.

Wilhelm Gruissem (W)

Department of Biology, Institute of Molecular Plant Biology, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland. wilhelm_gruissem@ethz.ch.
Advanced Plant Biotechnology Center, National Chung Hsing University, 145 Xingda Road, Taichung, 40227, Taiwan. wilhelm_gruissem@ethz.ch.

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Classifications MeSH