4.8 Article

Improved maize reference genome with single-molecule technologies

期刊

NATURE
卷 546, 期 7659, 页码 524-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nature22971

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资金

  1. NSF [IOS-1127112, 1444624]
  2. NSF Cereal Gene Discovery grant [1032105]
  3. USDA-ARS CRIS [1907-21000-030-00D]
  4. NSF Plant Genome award [1238014, 1444514]
  5. USDA Hatch project [CA-D-PLS-2066-H]
  6. USDA NIFA [HAW05022-H]
  7. NSF PGRP PRFB [1523793]
  8. Direct For Biological Sciences
  9. Division Of Integrative Organismal Systems [1238014, 1523793, 1444624, 1127112] Funding Source: National Science Foundation
  10. Division Of Integrative Organismal Systems
  11. Direct For Biological Sciences [1032105] Funding Source: National Science Foundation
  12. Div Of Molecular and Cellular Bioscience
  13. Direct For Biological Sciences [1444514] Funding Source: National Science Foundation

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Complete and accurate reference genomes and annotations provide fundamental tools for characterization of genetic and functional variation(1). These resources facilitate the determination of biological processes and support translation of research findings into improved and sustainable agricultural technologies. Many reference genomes for crop plants have been generated over the past decade, but these genomes are often fragmented and missing complex repeat regions(2). Here we report the assembly and annotation of a reference genome of maize, a genetic and agricultural model species, using single-molecule real-time sequencing and high-resolution optical mapping. Relative to the previous reference genome3, our assembly features a 52-fold increase in contig length and notable improvements in the assembly of intergenic spaces and centromeres. Characterization of the repetitive portion of the genome revealed more than 130,000 intact transposable elements, allowing us to identify transposable element lineage expansions that are unique to maize. Gene annotations were updated using 111,000 full-length transcripts obtained by single-molecule real-time sequencing(4). In addition, comparative optical mapping of two other inbred maize lines revealed a prevalence of deletions in regions of low gene density and maize lineage-specific genes.

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