Research Report

Quantitative Trait Locus Locating Analysis of Bud Set time in an F1 Hybrid Population of Populus deltoides and Populus simonii  

Chunfa Tong , Hainan Wu , Hua Gao , Deyuan Wang , Houxi Xu , Jiajia Ou , Ying Wang , Chunfa Tong
Co-Innovation Center for Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing, 210037
Author    Correspondence author
Tree Genetics and Molecular Breeding, 2020, Vol. 10, No. 4   doi: 10.5376/tgmb.2020.10.0004
Received: 20 Jul., 2020    Accepted: 27 Jul., 2020    Published: 14 Aug., 2020
© 2020 BioPublisher Publishing Platform
This article was first published in Molecular Plant Breeding in Chinese, and here was authorized to translate and publish the paper in English under the terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:

Zhao W., Wu H.N., Gao H., Wang D.Y., Xu H.X., Ou J.J., Wang Y., and Tong C.F., 2020, Quantitative trait locus locating analysis of bud set time in an F1 hybrid population of Populus deltoides and Populus simonii, Tree Genetics and Molecular Breeding, 10(4): 1-10 (doi: 10.5376/tgmb.2020.10.0004)

Growth and dormancy are the two most important biological processes in the life cycle of perennial plants. Studying dormancy-related traits is of great significance for understanding the adaptability of forest growth and improving the efficiency of plant molecular breeding. In order to reveal the genetic mechanism of poplar bud set, we performed quantitative trait locus (QTL) locating analysis of the trait with the KW method in the software MapQTL, based on the F1 hybrid population derived from a cross of Populus deltoides and Populus simonii and the two parental linkage maps. As a result, 15 QTLs controlling bud set were identified distributing on 7 linkage groups, among which 12 QTLs were located in linkage groups LG-1, LG-7, LG-9, LG-11 and LG-15 on the maternal P. deltoides map, whereas the other 3 QTLs were distributed in linkage groups LG-9 and LG-12 on the paternal P. simonii map. According to the location of the QTLs on the P. trichocarpa genome, a total of 45 candidate genes for bud set were identified. Furthermore, GO and KEGG enrichment analyses revealed that 71% of the candidate genes possessed potential functions in light and hormone signal transduction pathways. The research results provide a valuable resource for exploring the genes involved with bud set in poplar and for the application in molecular marker-assisted breeding.
Poplar; Bud set; QTL mapping; Candidate genes
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