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GrainGenes Sequence Report: CD453767

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Sequence	CD453767
Contig	Ta.19423.1.S1_a_at Ta.19423.1.S1_x_at Ta.19423.2.S1_a_at NSFT03P2_Contig18633
External Databases	Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index	TC295774
wEST map position	CD453767
NCBI UniGene	Ta.900
DB Remark	Locus Source: Triticum aestivum (bread wheat) UniGene title 'Transcribed locus, strongly similar to NP_001049811.1 Os03g0293500 [Oryza sativa (japonica cultivar-group)]'
Keyword	EST
Species	Triticum aestivum
Cultivar	Chinese Spring
Chromosome	2AS 4AS
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	WHE0874_G02_N04ZT CS wheat 20-45 DAP spike cDNA library Triticum aestivum cDNA clone WHE0874_G02_N04, mRNA sequence.
Strain	lab_host E. coli SOLR
Clone	WHE0874_G02_N04
Probe	WHE0874_G02_N04
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	tttttttttttttttagcgggggcaagctaaaaaatctcatgatcttctt agcattggcaggataaaacacaggcgatggccacagctcacaagtacagt aactagtaggcacaaaactaagaacataacagaagagcaaagataaactg ttcaacattatttgatggcaacgtgctgctggctgcgactactagtgatg caggcgtgcttggtctactgggggttgggtggcctggagttggcagcaga gaccctggagccccattccagaagctctttgctggtgtcgtccttgtgcg cgatcacctcgatgaagcacagagagtccttcttctcccccagcgccgtc tctatcgccgccgtcagctcctcctcgcacttcaccttggcagtccagca tttgccctccccgttgtggatggcctccacaagggcggtgtagttccagt tcttgatgacattgtaaggcccgtcgtggatctccacctcgatcgtgtac ccgccattgttgatcaggaagattatgccgttctgttcgcaccgcagcat agttgacacatcctgtgctgtcacctggaagctcccatcaccaatgcagg ctatgacacgcttgtcact

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