4.7 Article

Delineating the Tnt1 Insertion Landscape of the Model Legume Medicago truncatula cv. R108 at the Hi-C Resolution Using a Chromosome-Length Genome Assembly

期刊

出版社

MDPI
DOI: 10.3390/ijms22094326

关键词

Leguminosae; Medicago truncatula cv; R108; HiC; chromosome-length genome assembly; Tnt1 insertion landscape

资金

  1. NSF Physics Frontiers Center Award (Center for Theoretical Biological Physics) [PHY-1427654]
  2. Welch Foundation [Q-1866]
  3. Noble Research Institute, LLC.
  4. McNair Medical Institute Scholar Award
  5. NIH [U01HL130010]
  6. NIH Encyclopedia of DNA Elements (ENCODE) Mapping Center Award [UM1HG009375]
  7. NSF Plant Genome Grant [IOS-1733470]

向作者/读者索取更多资源

Legumes, especially Medicago truncatula, play a significant role in sustainable agricultural production by fixing atmospheric nitrogen to improve soil quality. While the Jemalong A17 accession of M. truncatula has a reference genome, the R108 accession is more favorable for genetic studies due to its high transformation efficiency and Tnt1-insertion population resource. The use of in situ Hi-C technology has allowed for the development of a chromosome-length genome assembly for M. truncatula cv. R108, facilitating accurate synteny analysis and providing insights for functional genomics research in legume crops.
Legumes are of great interest for sustainable agricultural production as they fix atmospheric nitrogen to improve the soil. Medicago truncatula is a well-established model legume, and extensive studies in fundamental molecular, physiological, and developmental biology have been undertaken to translate into trait improvements in economically important legume crops worldwide. However, M. truncatula reference genome was generated in the accession Jemalong A17, which is highly recalcitrant to transformation. M. truncatula R108 is more attractive for genetic studies due to its high transformation efficiency and Tnt1-insertion population resource for functional genomics. The need to perform accurate synteny analysis and comprehensive genome-scale comparisons necessitates a chromosome-length genome assembly for M. truncatula cv. R108. Here, we performed in situ Hi-C (48x) to anchor, order, orient scaffolds, and correct misjoins of contigs in a previously published genome assembly (R108 v1.0), resulting in an improved genome assembly containing eight chromosome-length scaffolds that span 97.62% of the sequenced bases in the input assembly. The long-range physical information data generated using Hi-C allowed us to obtain a chromosome-length ordering of the genome assembly, better validate previous draft misjoins, and provide further insights accurately predicting synteny between A17 and R108 regions corresponding to the known chromosome 4/8 translocation. Furthermore, mapping the Tnt1 insertion landscape on this reference assembly presents an important resource for M. truncatula functional genomics by supporting efficient mutant gene identification in Tnt1 insertion lines. Our data provide a much-needed foundational resource that supports functional and molecular research into the Leguminosae for sustainable agriculture and feeding the future.

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