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GrainGenes Sequence Report: NSFT03P2_Contig17512

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Sequence	CD453746
Contig	Ta.1055.2.S1_at Ta.1055.2.S1_x_at NSFT03P2_Contig17512
External Databases	Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index	TC278331
wEST map position	CD453746
NCBI UniGene	Ta.54729
DB Remark	Locus Source: Triticum aestivum (bread wheat) UniGene title 'Transcribed locus, moderately similar to NP_001058635.1 Os06g0727200 [Oryza sativa (japonica cultivar-group)]'
Keyword	EST
Species	Triticum aestivum
Cultivar	Chinese Spring
Chromosome	7AL 7BL 7DL
Clone Library	CS wheat 20-45 DAP spike cDNA library
Tissue	Spike and seed
Developmental Stage	Adult plant
Data Source	genbank Release 136, Jun 15 2003 genbank Updated Nov 2006
Title	WHE0859_D12_G23ZT CS wheat 20-45 DAP spike cDNA library Triticum aestivum cDNA clone WHE0859_D12_G23, mRNA sequence.
Strain	lab_host E. coli SOLR
Clone	WHE0859_D12_G23
Probe	MAG1714 WHE0859_D12_G23
Remark	DB_xref: taxon:4565 Feature: source: mol_type = 'mRNA'; Locus Comment: Contact: Olin Anderson; US Department of Agriculture, Agriculture Research Service, Pacific; West Area, Western Regional Research Center; 800 Buchanan Street, Albany, CA 94710, USA; Tel: 5105595773; Fax: 5105595818; Email: oandersn@pw.usda.gov; This EST was generated by sequencing from the 3' end of the clone.; Sequences have been trimmed to remove vector sequence and low; quality sequence with phred score less than 20.; Seq primer: T7 primer. Note: Vector: Lambda Uni-ZAP XR, excised phagemid; Site_1: EcoRI; Site_2: XhoI; Plants were grown in the greenhouse. Spikes at 20 DAP and seeds at 30 to 45 DAP were harvested, total RNA and poly(A) RNA were prepared, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab (Choi, Close, Fenton) at the University of California, Riverside. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors ). Note: Vector: Lambda Uni-ZAP XR, excised phagemid; Site_1: EcoRI; Site_2: XhoI; Plants were grown in the greenhouse. Spikes at 20 DAP and seeds at 30 to 45 DAP were harvested, total RNA and poly(A) RNA were prepared, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab (Choi, Close, Fenton) at the University of California, Riverside. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA	ttttttttaaaccaacacattgtcttttattttcccttttgcacagacac aatacgacagacgaactgtatcacaacacccaccatcatgggtattacat acaatattcattacacatttttattcatggctacacccacacagagacag attcagttcatgctgcaccctccttggctcgatcgacgccaaccgaggcg ggtgagcgactggttccctcctccttttccatctacatgctcggcttaat cttgagccgcgatgccagcttcttcccgagggacgcgtcacactgtgacc agtatgagacccagatgccctggatttcatgggtaacacgagcatcagtg agcgcatcaacccagcgctgtaggaaacggtcttgcctggcagggccgaa ggaacggtatctctcgccagcctgcttgaaattgttctccttttcgatga tgcacttctcccggcagccaaataaaacgcgaggagggacagggtactgt tcagcatgacgagtaggatcaaaccttgaagggaagtagttcacctcctc atccctgtgcatgaaattcattaagccatcatgatggttgttgtggtg

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