Gossypium barbadense (AD2) '3-79' genome HAU_v1
About the assembly
Here, we report the genome sequence of the superior fibre quality tetraploid cotton, G. barbadense acc. 3-79 using a whole-genome shotgun approach with large fragments of DNA Paired-End Tag (DNA-PET) sequencing data. This is a high-quality assembly of the 2.57 gigabase genome of G. barbadense, including 80,876 protein-coding genes. The double-sized genome of the A (or At) (1.50 Gb) against D (or Dt) (853 Mb) primarily resulted from the expansion of Gypsy elements, including Peabody and Retrosat2 subclades in the Del clade, and the Athila subclade in the Athila/Tat clade. Substantial gene expansion and contraction were observed and rich homoeologous gene pairs with biased expression patterns were identified, suggesting abundant gene sub-functionalization occurred by allopolyploidization. More specifically, the CesA gene family has adapted differentially temporal expression patterns, suggesting an integrated regulatory mechanism of CesA genes from At and Dt subgenomes for the primary and secondary cellulose biosynthesis of cotton fibre in a “relay race”-like fashion. It is anticipated that the G. barbadense genome sequence will advance the understanding of the mechanism of genome polyploidization and underpin genome-wide comparison research in this genus.
Yuan et.al, The genome sequence of Sea-Island cotton (Gossypium barbadense) provides insights into the allopolyploidization and development of superior spinnable fibres. Sci Rep. 2015 Dec 4;5:17662. doi: 10.1038/srep17662.
Additional information about this analysis:
The chromosomes (pseudomolecules) and scaffolds for Gossypium barbadense (AD1) Genome HAU-NBI Assembly v1.0
All assembly and annotation files are available for download by selecting the desired data type in the left-hand side bar. Each data type page will provide a description of the available files and links to download.
Functional annotation for Gossypium barbadense (AD2) Genome NBI Assembly v1.0 (Performed by NBI)
Functional annotation for Gossypium barbadense (AD2) Genome NBI Assembly v1.0 (Performed by the CottonGen Team of the Main Bioinformatics Lab at WSU.)
The predicted genes and proteins for Gossypium barbadense (AD2) Genome HAU-NBI Assembly v1.0
Marker alignments were performed by the CottonGen Team of Main Bioinformatics Lab at WSU. The alignment tool 'BLAT' was used to map marker sequences from CottonGen to the G. barbadense genome assembly. Markers required 90% identity over 97% of their length. For SSRs & RFLPs, gap size was restricted to 1000bp or less with less than 2 gaps. For dbSNPs and Indels gap size was restricted to 2bp with less than 2 gaps. The available files are in GFF3 format. Markers available in CottonGen and CMap are linked to JBrowse.
Homology of the Gossypium barbadense HAU v1.0 proteins was determined by pairwise sequence comparison using the blastp algorithm against various protein databases. An expectation value cutoff less than 1e-9 was used for the NCBI nr (Release 2018-05) and 1e-6 for the Arabidoposis proteins (Araport11), UniProtKB/SwissProt (Release 2019-01), and UniProtKB/TrEMBL (Release 2019-01) databases. The best hit reports are available for download in Excel format.
Transcript alignments were performed by the CottonGen Team of Main Bioinformatics Lab at WSU. The alignment tool 'BLAT' was used to map transcripts to the G. barbadense genome assembly. Alignments with an alignment length of 97% and 98% identify were preserved. The available files are in GFF3 format.