Optical and physical mapping with local finishing enables megabase-scale resolution of agronomically important regions in the wheat genome
Authors:
- Gabriel Keeble-GagnèreGKGabriel Keeble-Gagnère
- Philippe RigaultPRPhilippe Rigault
- Josquin TibbitsJTJosquin Tibbits
- Raj PasamRPRaj Pasam
- Matthew HaydenMHMatthew Hayden
- Kerrie ForrestKFKerrie Forrest
- Zeev FrenkelZFZeev Frenkel
- Abraham KorolAKAbraham Korol
- Emma HuangEHEmma Huang
- Colin CavanaghCCColin Cavanagh
- Jen TaylorJTJen Taylor
- Michael AbroukMAMichael Abrouk
Preprint
Abstract
Background: Numerous scaffold-level sequences for wheat are now being released and, in this context, we report on a strategy for improving the overall assembly to a level comparable to that of the human genome. Results: Using chromosome 7A of wheat as a model, sequence-finished megabase scale sections of this chromosome were established by combining a new independent assembly based on a BAC-based physical map, BAC pool paired end sequencing, chromosome arm specific mate-pair sequencing and Bionano optical mapping with the IWGSC RefSeq v1.0 sequence and its underlying raw data. The combined assembly results in 18 super-scaffolds across the chromosome. The value of finished genome regions is demonstrated for two approximately 2.5 Mb regions associated with yield and the grain quality phenotype of fructan carbohydrate grain levels. In addition, the 50 Mb centromere region analysis incorporates cytological data highlighting the importance of non-sequence data in the assembly of this complex genome region. Conclusions: Sufficient genome sequence information is shown to be now available for the wheat community to produce sequence-finished releases of each chromosome of the reference genome. The high-level completion identified that an array of seven fructosyl transferase genes underpins grain quality and yield attributes are affected by five f-box-only-protein-ubiquitin ligase domain and four root-specific lipid transfer domain genes. The completed sequence also includes the centromere.Keywords
All Related Versions
- Published version: Genome Biology, 19 (1), 1.
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