| Literature DB >> 32081276 |
Jiaojiao Ren1, Nicholas A Boerman2, Ruixiang Liu3, Penghao Wu1, Benjamin Trampe2, Kimberly Vanous2, Ursula K Frei2, Shaojiang Chen4, Thomas Lübberstedt5.
Abstract
In vivo doubled haploid (DH) technology is widely used in commercial maize (Zea mays L.) breeding. Haploid genome doubling is a critical step in DH breeding. In this study, inbred lines GF1 (0.65), GF3(0.29), and GF5 (0) with high, moderate, and poor spontaneous haploid genome doubling (SHGD), respectively, were selected to develop mapping populations for SHGD. Three QTL, qshgd1, qshgd2, and qshgd3, related to SHGD were identified by selective genotyping. With the exception of qshgd3, the source of haploid genome doubling alleles were derived from GF1. Furthermore, RNA-Seq was conducted to identify putative candidate genes between GF1 and GF5 within the qshgd1 region. A differentially expressed formin-like protein 5 transcript was identified within the qshgd1 region.Entities:
Keywords: Doubled haploid (DH); Maize; RNA-seq; Spontaneous haploid genome doubling (SHGD)
Year: 2019 PMID: 32081276 DOI: 10.1016/j.plantsci.2019.110337
Source DB: PubMed Journal: Plant Sci ISSN: 0168-9452 Impact factor: 4.729