Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Jan;80(1):138-146.
doi: 10.1161/HYPERTENSIONAHA.122.20140. Epub 2022 Nov 4.

The Assembled Genome of the Stroke-Prone Spontaneously Hypertensive Rat

Affiliations

The Assembled Genome of the Stroke-Prone Spontaneously Hypertensive Rat

Theodore S Kalbfleisch et al. Hypertension. 2023 Jan.

Abstract

Background: We report the creation and evaluation of a de novo assembly of the genome of the spontaneously hypertensive rat, the most widely used model of human cardiovascular disease.

Methods: The genome is assembled from long read sequencing (PacBio HiFi and continuous long read data [CLR]) and scaffolded with long-range structural information obtained from Bionano optical maps and proximity ligation sequencing proximity analysis of the genome. The genome assembly was polished with Illumina short reads. Completeness of the assembly was investigated using Benchmarking Universal Single Copy Orthologs analysis. The genome assembly was also evaluated with the rat reference gene set, using NCBI automated protocols. We also generated orthogonal single molecule transcript sequence reads (Iso-Seq) from 8 tissues and used them to validate the coding assembly, to annotate the assembly with RNA transcripts representing unique full length transcript isoforms for each gene and to determine whether divergences between RefSeq sequences and the assembly were attributable to assembly errors or polymorphisms.

Results: The assembly analysis indicates that this assembly is comparable in contiguity and completeness to the current rat reference assembly, while the use of HiFi sequencing yields an assembly that is more correct at the single base level. Synteny analysis was performed to uncover the extent of synteny and the presence and distribution of chromosomal rearrangements between the reference and this assembly.

Conclusion: The resulting genome assembly is reference quality and captures significant structural variation.

Keywords: cardiovascular diseases; genomics; spontaneously hypertensive rat; synteny; whole genome sequencing.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Visual representation of mRatBN7.2 and SHRSP genome assemblies made using assembly-stats software.
Figure 2
Figure 2
Synteny and Rearrangement plot of the current rat reference (mRatBN7.2) compared with the SHRSP genome assembly. This plot reveals both within and across chromosome re-arrangements.

References

    1. Gibbs RA, Weinstock GM, Metzker ML, Muzny DM, Sodergren EJ, Scherer S, et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature 2004;428: 493–521. doi:10.1038/nature02426 - DOI - PubMed
    1. Jeffet J, Margalit S, Michaeli Y, Ebenstein Y. Single-molecule optical genome mapping in nanochannels: multidisciplinarity at the nanoscale. Essays Biochem 2021;65: 51–66. doi:10.1042/EBC20200021 - DOI - PMC - PubMed
    1. Ghurye J, Rhie A, Walenz BP, Schmitt A, Selvaraj S, Pop M, et al. Integrating Hi-C links with assembly graphs for chromosome-scale assembly. PLoS Comput Biol 2019;15: e1007273. doi:10.1371/journal.pcbi.1007273 - DOI - PMC - PubMed
    1. Howe K, Dwinell M, Shimoyama M, Corton C, Betteridge E, Dove A, et al. The genome sequence of the Norway rat, Rattus norvegicus Berkenhout 1769. Wellcome Open Res 2021;6: 118. doi:10.12688/wellcomeopenres.16854.1 - DOI - PMC - PubMed
    1. Martiniano R, Garrison E, Jones ER, Manica A, Durbin R. Removing reference bias and improving indel calling in ancient DNA data analysis by mapping to a sequence variation graph. Genome Biol 2020;21: 250. doi:10.1186/s13059-020-02160-7 - DOI - PMC - PubMed

Publication types