Mapping a candidate gene (MdMYB10) for red flesh and foliage colour in apple
Open Access
- 1 January 2007
- journal article
- Published by Springer Nature in BMC Genomics
- Vol. 8 (1), 212
- https://doi.org/10.1186/1471-2164-8-212
Abstract
Integrating plant genomics and classical breeding is a challenge for both plant breeders and molecular biologists. Marker-assisted selection (MAS) is a tool that can be used to accelerate the development of novel apple varieties such as cultivars that have fruit with anthocyanin through to the core. In addition, determining the inheritance of novel alleles, such as the one responsible for red flesh, adds to our understanding of allelic variation. Our goal was to map candidate anthocyanin biosynthetic and regulatory genes in a population segregating for the red flesh phenotypes.Keywords
This publication has 31 references indexed in Scilit:
- Red colouration in apple fruit is due to the activity of the MYB transcription factor, MdMYB10The Plant Journal, 2007
- Light-Induced Expression of a MYB Gene Regulates Anthocyanin Biosynthesis in Red ApplesPlant Physiology, 2006
- Development and linkage mapping of E-STS and RGA markers for functional gene homologues in appleGenome, 2006
- Plant bioinformatics: from genome to phenomeTrends in Biotechnology, 2004
- Candidate gene analysis of anthocyanin pigmentation loci in the SolanaceaeTheoretical and Applied Genetics, 2003
- Major Phenolics in Apple and Their Contribution to the Total Antioxidant CapacityJournal of Agricultural and Food Chemistry, 2003
- Analysis of bHLH and MYB domain proteins: species‐specific regulatory differences are caused by divergent evolution of target anthocyanin genesThe Plant Journal, 1998
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Analysis of Arabidopsis mutants deficient in flavonoid biosynthesisThe Plant Journal, 1995
- Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specific genomic regions by using segregating populations.Proceedings of the National Academy of Sciences, 1991