A global assembly of cotton ESTs

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 cott...

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Published in:Genome Research Vol. 16; no. 3; pp. 441 - 450
Main Authors: 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
Format: Journal Article
Language:English
Published: United States Cold Spring Harbor Laboratory Press 01-03-2006
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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; A(T) and D(T) 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.
AbstractList 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 ; A T and D T 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.
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; A(T) and D(T) 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.
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; A(T) and D(T) 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.
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; A sub(T) and D sub(T) 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.
Author Wendel, Jonathan F
Chen, Xiao Ya
Kudrna, David
Wilkins, Thea A
Guo, Jin Ying
Yu, Yeisoo
Arpat, Aladdin B
Zhang, Deshui
Wu, Yingru
Pierce, Margaret L
Essenberg, Margaret
Rapp, Ryan A
Dowd, Caitriona
Kim, Hyeran
Allen, Randell
Swanson, Jordan M
Wing, Rod
Paterson, Andrew H
Schulze, Stefan R
Taliercio, Earl
Turley, Ricky
Dennis, Elizabeth S
Sickler, Brad A
Soderlund, Cari
McFadden, Helen
Hatfield, Jamie
Klueva, Natalya
Payton, Paxton
Suo, Jinfeng
Sparks, Michael E
Llewellyn, Danny J
Wilkerson, Curtis
Udall, Joshua A
Scheffler, Jodi
Haller, Karl
Haigler, Candace
AuthorAffiliation 1 Department of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, Iowa 50011, USA
14 Oklahoma Agricultural Experiment Station, Oklahoma State University, Stillwater, Oklahoma 74078, USA
6 Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Shanghai, 200032, China
5 Department of Plant Sciences, University of California–Davis, Davis, California 95616, USA
12 Institute of Genetics and Developmental Biology, Beijing, 100101, China
7 United States Department of Agriculture–Agricultural Research Service, Stoneville, Mississippi 38776, USA
9 Department of Biology, Texas Tech University, Lubbock, Texas 79409, USA
4 CSIRO Plant Industry, Canberra City ACT 2601, Australia
11 Bioinformatics Core Facility, Michigan State University, East Lansing, Michigan 48824, USA
8 United States Department of Agriculture–Agricultural Research Service, Lubbock, Texas 79415, USA
13 Plant Genome Mapping Laboratory, University of Georgia, Athens, Georgia 30602, USA
2
AuthorAffiliation_xml – name: 4 CSIRO Plant Industry, Canberra City ACT 2601, Australia
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– name: 12 Institute of Genetics and Developmental Biology, Beijing, 100101, China
– name: 3 Arizona Genomics Institute, Department of Plant Sciences, University of Arizona, Tucson, Arizona 85721, USA
– name: 6 Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Shanghai, 200032, China
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– name: 7 United States Department of Agriculture–Agricultural Research Service, Stoneville, Mississippi 38776, USA
– name: 10 Department of Crop Science and Department of Botany, North Carolina State University, Raleigh, North Carolina 27695, USA
– name: 2 Arizona Genomics Computational Laboratory, BIO5 Institute, University of Arizona, Tucson, Arizona 85721, USA
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  surname: Udall
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  organization: Department of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, Iowa 50011, USA
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  fullname: Taliercio, Earl
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  fullname: Turley, Ricky
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  fullname: McFadden, Helen
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  fullname: Payton, Paxton
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  fullname: Klueva, Natalya
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  fullname: Allen, Randell
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  surname: Suo
  fullname: Suo, Jinfeng
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  givenname: Stefan R
  surname: Schulze
  fullname: Schulze, Stefan R
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  surname: Pierce
  fullname: Pierce, Margaret L
– sequence: 28
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  surname: Essenberg
  fullname: Essenberg, Margaret
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  fullname: Kim, Hyeran
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  givenname: Danny J
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– sequence: 31
  givenname: Elizabeth S
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  fullname: Dennis, Elizabeth S
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  givenname: Rod
  surname: Wing
  fullname: Wing, Rod
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  givenname: Andrew H
  surname: Paterson
  fullname: Paterson, Andrew H
– sequence: 35
  givenname: Cari
  surname: Soderlund
  fullname: Soderlund, Cari
– sequence: 36
  givenname: Jonathan F
  surname: Wendel
  fullname: Wendel, Jonathan F
BackLink https://www.ncbi.nlm.nih.gov/pubmed/16478941$$D View this record in MEDLINE/PubMed
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Corresponding author.…E-mail jfw@iastate.edu; fax (515) 294-1337.
Article published online ahead of print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.4602906.
Supplemental material is available online at www.genome.org. The ESTs from GR_Ea and GR_Eb were deposited in GenBank under accession nos. CO069431–CO100583 and CO100584–CO132899.
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PublicationTitle Genome Research
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Snippet Approximately 185,000 Gossypium EST sequences comprising >94,800,000 nucleotides were amassed from 30 cDNA libraries constructed from a variety of tissues and...
Approximately 185,000 Gossypium EST sequences comprising >94,800,000 nucleotides were amassed from 30 cDNA libraries constructed from a variety of tissues and...
Approximately 185,000 Gossypium EST sequences comprising >94,800,000 nucleotides were amassed from 30 cDNA libraries constructed from a variety of tissues...
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SubjectTerms Diploidy
DNA, Complementary - genetics
Expressed Sequence Tags
Gene Expression Profiling - methods
Genome, Plant
Gossypium - genetics
Gossypium arboreum
Gossypium hirsutum
Gossypium raimondii
Molecular Sequence Data
Polyploidy
Resources
Sequence Analysis, DNA
Title A global assembly of cotton ESTs
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