Sporobolus pyramidalis v1 Assembly & Annotation

Overview

Analysis Name Sporobolus pyramidalis v1 Assembly & Annotation
Sequencing technology Illumina, Hi-C
Assembly method Meraculous
Release Date 2022-01-26
Reference Publication(s)

Chávez Montes RA, Haber A, Pardo J, Powell RF, Divisetty UK, Silva AT, Hernández-Hernández T, Silveira V, Tang H, Lyons E, Herrera Estrella LR, VanBuren R, Oliver MJ. A comparative genomics examination of desiccation tolerance and sensitivity in two sister grass species. Proc Natl Acad Sci U S A. 2022 Feb 1;119(5):e2118886119. doi: 10.1073/pnas.2118886119.

Abstract

Desiccation tolerance is an ancient and complex trait that spans all major lineages of life on earth. Although important in the evolution of land plants, the mechanisms that underlay this complex trait are poorly understood, especially for vegetative desiccation tolerance (VDT). The lack of suitable closely related plant models that offer a direct contrast between desiccation tolerance and sensitivity has hampered progress. We have assembled high-quality genomes for two closely related grasses, the desiccation-tolerant Sporobolus stapfianus and the desiccation-sensitive Sporobolus pyramidalis. Both species are complex polyploids; S. stapfianus is primarily tetraploid, and S. pyramidalis is primarily hexaploid. S. pyramidalis undergoes a major transcriptome remodeling event during initial exposure to dehydration, while S. stapfianus has a muted early response, with peak remodeling during the transition between 1.5 and 1.0 grams of water (gH2O) g−1 dry weight (dw). Functionally, the dehydration transcriptome of S. stapfianus is unrelated to that for S. pyramidalis. A comparative analysis of the transcriptomes of the hydrated controls for each species indicated that S. stapfianus is transcriptionally primed for desiccation. Cross-species comparative analyses indicated that VDT likely evolved from reprogramming of desiccation tolerance mechanisms that evolved in seeds and that the tolerance mechanism of S. stapfianus represents a recent evolution for VDT within the Chloridoideae. Orthogroup analyses of the significantly differentially abundant transcripts reconfirmed our present understanding of the response to dehydration, including the lack of an induction of senescence in resurrection angiosperms. The data also suggest that failure to maintain protein structure during dehydration is likely critical in rendering a plant desiccation sensitive.

Assembly statistics

Assembly size, bp1,055,099,634
No. of contigs2,518
Longest contig, bp60,313,943
N5021,593,735
N907,502,351
Assembly levelChromosome

Assembly

The Sporobolus pyramidalis v1 Assembly file is available in FASTA format.

Downloads

Chromosomes (FASTA file) Sporobolus_pyramidalis.faa.gz

Gene Predictions

The Sporobolus pyramidalis v1 genome gene prediction files are available in GFF3 and FASTA format.

Downloads

Genes (GFF3 file) Sporobolus_pyramidalis.gff.gz
CDS sequences (FASTA file) Sp_cds.fa.gz
Protein sequences (FASTA file) Sp_pep.fa.gz

Functional Analysis

Functional annotation for the Sporobolus pyramidalis v1 is available for download below. The proteins were analyzed using InterProScan to assign InterPro domains(Pfam).

Downloads

Domain from InterProScan Sporobolus_pyramidalis.Pfam.tsv.gz

S genes

Summary

QueryScaffoldSize(bp)CoordinatestBLASTn HittBLASTn %IDDomain
DUF247I-SΨScaffold24785038051117826504-17827964Cpurpureus64DUF247
DUF247II-S1Scaffold15278542109982614-9984242CgayanaS259DUF247
DUF247II-S2Scaffold25175528835440178084-40179694CgayanaS259DUF247
HPS10-SScaffold24785038051117843191-17843326,
17843445-17843563
SspontaneumS280-
DUF247I-Z1Scaffold4882471023167908-3169509LpZDUF247-I_chromosome261DUF247
DUF247I-Z2Scaffold4882471023715774-3717381LpZDUF247-I_chromosome261DUF247
DUF247II-Z1ΨScaffold615334402114029-114274Eindica69DUF247
DUF247II-Z2Scaffold4882471023709712-3711340Eindica80DUF247
HPS10-Z1Scaffold615334402121291-121480,
121561-121664
AerianthaHPS10-Z71-
HPS10-Z2Scaffold4882471023713514-3713598,
3713811-3713917
CsongoricaZ241-

Nucleotide

Protein

© 2023 National Genomics Data Center, China National Center for Bioinformation / Beijing Institute of Genomics, Chinese Academy of Sciences