Author:
Udall Joshua A.,Swanson Jordan M.,Haller Karl,Rapp Ryan A.,Sparks Michael E.,Hatfield Jamie,Yu Yeisoo,Wu Yingru,Dowd Caitriona,Arpat Aladdin B.,Sickler Brad A.,Wilkins Thea A.,Guo Jin Ying,Chen Xiao Ya,Scheffler Jodi,Taliercio Earl,Turley Ricky,McFadden Helen,Payton Paxton,Klueva Natalya,Allen Randell,Zhang Deshui,Haigler Candace,Wilkerson Curtis,Suo Jinfeng,Schulze Stefan R.,Pierce Margaret L.,Essenberg Margaret,Kim HyeRan,Llewellyn Danny J.,Dennis Elizabeth S.,Kudrna David,Wing Rod,Paterson Andrew H.,Soderlund Cari,Wendel Jonathan F.
Abstract
Approximately 185,000 Gossypium EST sequences comprising >94,800,000 nucleotides were amassed from 30 cDNA libraries constructed from a variety of tissues and organs under a range of conditions, including drought stress and pathogen challenges. These libraries were derived from allopolyploid cotton (Gossypium hirsutum; AT and DT genomes) as well as its two diploid progenitors, Gossypium arboreum (A genome) and Gossypium raimondii (D genome). ESTs were assembled using the Program for Assembling and Viewing ESTs (PAVE), resulting in 22,030 contigs and 29,077 singletons (51,107 unigenes). Further comparisons among the singletons and contigs led to recognition of 33,665 exemplar sequences that represent a nonredundant set of putative Gossypium genes containing partial or full-length coding regions and usually one or two UTRs. The assembly, along with their UniProt BLASTX hits, GO annotation, and Pfam analysis results, are freely accessible as a public resource for cotton genomics. Because ESTs from diploid and allotetraploid Gossypium were combined in a single assembly, we were in many cases able to bioinformatically distinguish duplicated genes in allotetraploid cotton and assign them to either the A or D genome. The assembly and associated information provide a framework for future investigation of cotton functional and evolutionary genomics.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics(clinical),Genetics