摘要
Future breeding programs have to meet diverse demands of different consumers, which require massive genetic resources and variations. However, the number of natural existing haplotypes is always limited due to domestication and breeding process (Tanksley and Mc Couch, 1997). Compared with traditional genetic cloning approaches, elucidating how one gene is transcribed and how it regulates downstream workhorses will generate more information on the casual mutation(s) of the gene and its downstream targets.
基金
supported by the National Transgenic Science and Technology Program(2019ZX08010-003)。
