| Literature DB >> 30061736 |
Nathan M Springer1, Sarah N Anderson1, Carson M Andorf2, Kevin R Ahern3, Fang Bai4, Omer Barad5, W Brad Barbazuk6, Hank W Bass7, Kobi Baruch5, Gil Ben-Zvi5, Edward S Buckler8,9, Robert Bukowski9, Michael S Campbell10, Ethalinda K S Cannon2, Paul Chomet5, R Kelly Dawe11, Ruth Davenport6, Hugo K Dooner12,13, Limei He Du12,13, Chunguang Du14, Katherine A Easterling7, Christine Gault6, Jiahn-Chou Guan4, Charles T Hunter15, Georg Jander3, Yinping Jiao10, Karen E Koch4, Guy Kol5, Tobias G Köllner16, Toru Kudo4,17, Qing Li1, Fei Lu9,18,19, Dustin Mayfield-Jones20, Wenbin Mei6, Donald R McCarty4, Jaclyn M Noshay1, John L Portwood2, Gil Ronen5, A Mark Settles4, Doron Shem-Tov5, Jinghua Shi21, Ilya Soifer5, Joshua C Stein10, Michelle C Stitzer22, Masaharu Suzuki4, Daniel L Vera23, Erik Vollbrecht24, Julia T Vrebalov3, Doreen Ware8,10,25, Sharon Wei10, Kokulapalan Wimalanathan24, Margaret R Woodhouse2, Wenwei Xiong14, Thomas P Brutnell26,27.
Abstract
The maize W22 inbred has served as a platform for maize genetics since the mid twentieth century. To streamline maize genome analyses, we have sequenced and de novo assembled a W22 reference genome using short-read sequencing technologies. We show that significant structural heterogeneity exists in comparison to the B73 reference genome at multiple scales, from transposon composition and copy number variation to single-nucleotide polymorphisms. The generation of this reference genome enables accurate placement of thousands of Mutator (Mu) and Dissociation (Ds) transposable element insertions for reverse and forward genetics studies. Annotation of the genome has been achieved using RNA-seq analysis, differential nuclease sensitivity profiling and bisulfite sequencing to map open reading frames, open chromatin sites and DNA methylation profiles, respectively. Collectively, the resources developed here integrate W22 as a community reference genome for functional genomics and provide a foundation for the maize pan-genome.Entities:
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Year: 2018 PMID: 30061736 DOI: 10.1038/s41588-018-0158-0
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330