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GrainGenes Sequence Report: BQ172287

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Sequence	BQ172287
Contig	Ta.28081.1.S1_at NSFT03P2_Contig11726
External Databases	Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index	TC282432
wEST map position	BQ172287
NCBI UniGene	Ta.28081
DB Remark	Locus Source: Triticum aestivum (bread wheat) UniGene title 'Clone wlm24.pk0016.f9:fis, full insert mRNA sequence'
Keyword	EST
Species	Triticum aestivum
Cultivar	Chinese Spring
Chromosome	2AL 2BL 2DL
Clone Library	Wheat salt-stressed sheath cDNA library
Tissue	Sheath
Developmental Stage	Adult plant
Data Source	genbank Release 135, Apr 15 2003 genbank Updated Nov 2006
Title	WHE2057_H05_P09ZT Wheat salt-stressed sheath cDNA library Triticum aestivum cDNA clone WHE2057_H05_P09, mRNA sequence.
Strain	lab_host E. coli SOLR
Clone	WHE2057_H05_P09
Probe	WHE2057_H05_P09
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 under hydroponic conditions at UC Davis, salt stressed for 12 hours, and for 7 days, then dissected and frozen (Akhunov in J Dvorak Lab). Total RNA was prepared from sheath tissue, equal quantities of RNA were pooled from the two samples, polyA was purified from the pooled RNA, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab at the University of California, Riverside (Akhunov, Chin , Choi, Close, Fenton, Kianian, Otto, Simons, Zhang). 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 under hydroponic conditions at UC Davis, salt stressed for 12 hours, and for 7 days, then dissected and frozen (Akhunov in J Dvorak Lab). Total RNA was prepared from sheath tissue, equal quantities of RNA were pooled from the two samples, polyA was purified from the pooled RNA, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab at the University of California, Riverside (Akhunov, Chin, Choi, Close, Fenton, Kianian, Otto, Simons, Zhang). Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA	ttttttttttttttttttacgcttccaacaagagaacaattgcattgcaa accttgccgattttgcggttagtgaatattggccggtctacacaaggctg ctaattaattaagctccgaaattaacaccataaacaaaggggaataatca ctgccagcagtggcgagcattctgaaatctgaaacctcgactaatcactc agctaaggtgtgcgatgtcgacctcgtcaggtaacttgaaggtatccgca gccccaaacttcttcctcccctccttccactcgtcctcgtcctccaggct gtcgctgtcgtcgttctcatgcccgtggcttgatggagtcatagggtcct caacactctttgacttgcagtggccgttggcgagcatggtgacctggcgg aggtgggagatctcgacgactacggtctcgtcgttgctggggagtggctg cttccatggttcgccgtcgaccctcatgaacgtgtggtcgggtgctcctt tg

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