作者
Wenbin Guo,Miriam Schreiber,Vanda B. Marosi,Paolo Bagnaresi,Morten Egevang Jørgensen,Katarzyna Braune,K. J. Chalmers,Brett Chapman,Viet Hoang Dang,Christoph Dockter,Anne Fiebig,Geoffrey B. Fincher,Agostino Fricano,John Fuller,Allison Haaning,Georg Haberer,Axel Himmelbach,Murukarthick Jayakodi,Yong Jia,Nadia Kamal,Peter Langridge,Chengdao Li,Qiongxian Lu,Thomas Lux,Martin Mascher,Klaus Mayer,Nicola McCallum,Linda Milne,Gary J. Muehlbauer,Martin Toft Simmelsgaard Nielsen,Sudharsan Padmarasu,Pai Pedas,Klaus Pillen,Curtis Pozniak,Magnus Wohlfahrt Rasmussen,Kazuhiro Sato,Thomas Schmutzer,Uwe Scholz,Danuta Schüler,Hana Šimková,Birgitte Skadhauge,Nils Stein,Nina W. Thomsen,Cynthia Voss,Penghao Wang,Ronja Wonneberger,Xiaoqi Zhang,Guoping Zhang,Luigi Cattivelli,M. Spannagl,Micha Bayer,Craig G. Simpson,Runxuan Zhang,Robbie Waugh
摘要
Abstract A pan-transcriptome describes the transcriptional and post-transcriptional consequences of genome diversity from multiple individuals within a species. We developed a barley pan-transcriptome using 20 inbred genotypes representing domesticated barley diversity by generating and analyzing short- and long-read RNA-sequencing datasets from multiple tissues. To overcome single reference bias in transcript quantification, we constructed genotype-specific reference transcript datasets (RTDs) and integrated these into a linear pan-genome framework to create a pan-RTD, allowing transcript categorization as core, shell or cloud. Focusing on the core (expressed in all genotypes), we observed significant transcript abundance variation among tissues and between genotypes driven partly by RNA processing, gene copy number, structural rearrangements and conservation of promotor motifs. Network analyses revealed conserved co-expression module::tissue correlations and frequent functional diversification. To complement the pan-transcriptome, we constructed a comprehensive cultivar (cv.) Morex gene-expression atlas and illustrate how these combined datasets can be used to guide biological inquiry.