LOCUS BE470556 603 bp mRNA linear EST 28-JUL-2000
DEFINITION WHE0261_C03_C03ZS Wheat drought-stressed seedling cDNA library
Triticum aestivum cDNA clone WHE0261_C03_C03, mRNA sequence.
ACCESSION BE470556
VERSION BE470556.1
DBLINK BioSample: SAMN00160041
KEYWORDS EST.
SOURCE Triticum aestivum (bread wheat)
ORGANISM Triticum aestivum
Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
Spermatophyta; Magnoliopsida; Liliopsida; Poales; Poaceae; BOP
clade; Pooideae; Triticodae; Triticeae; Triticinae; Triticum.
REFERENCE 1 (bases 1 to 603)
AUTHORS Anderson,O.D., Chao,S., Choi,D.W., Close,T.J., Fenton,R.D.,
Han,P.S., Hsia,C.C., Kang,Y., Lazo,G.R., Miller,R., Rausch,C.J.,
Seaton,C.L. and Tong,J.C.
TITLE The structure and function of the expressed portion of the wheat
genomes - Drought-stressed seedling cDNA library
JOURNAL Unpublished
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
Sequence have been trimmed to remove vector sequence and low
quality sequence with phred score less than 20
Seq primer: Stratagene SK primer.
FEATURES Location/Qualifiers
source 1..603
/organism="Triticum aestivum"
/mol_type="mRNA"
/cultivar="Chinese Spring"
/db_xref="taxon:4565"
/clone="WHE0261_C03_C03"
/tissue_type="Seedling without endosperm"
/clone_lib="SAMN00160041 Wheat drought-stressed seedling
cDNA library"
/dev_stage="Five day old seedling"
/lab_host="E. coli SOLR"
/note="Vector: Lambda Uni-ZAP XR, excised phagemid;
Site_1: EcoRI; Site_2: XhoI; Seeds were
surface-sterilized, germinated and grown aseptically in
the dark at room temperature on filter paper with water,
nystatin and cefotaxime in covered crystallization dishes.
Five-day old seedlings were incubated for one day at 90%
RH. After removing endosperm, seedlings were transferred
to desiccator jar containing saturated MgSO4 at room
temperature for 24 hr. The tissue, 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)."
BASE COUNT 162 a 153 c 160 g 128 t
ORIGIN
1 gccgggatca gatccatctc tccgcgcgcg atgtctgagg tggcagcgac ggcggggcag
61 gcgtacatga gacagctctc caagcacccg ctccgcacca aggccatcac ctccggggtg
121 ctggccggct gcagcgacgc cgtcgcccag aagatctccg gcgtcaagaa gctccagctc
181 aggaggctcc tcctcataat gctctatgga tttgcatacg caggaccatt cggtcatttt
241 ttccacaagc ttatggacaa gattttcaag ggacagaaga aaggaaaaga aactacagcc
301 aagaaggtca tagtggagca gctaactgta tcaccatgga acaatatgat gttcatgatg
361 tactacggtc tggtagttga agggaggcca ttcgggcaag taaagagcaa ggtcaagaag
421 gactttgcaa acatccaatt gacagcttgg aagttctggc caatagttag ctggatcaat
481 tatgagtaca tgccactcca gctccgagtt cttttcgcca gctccgttgc atcatgctgg
541 gcagtgtttc tgaacctgaa agcagcaaga tccattgccg gcactagtaa gaatgcataa
601 aag
//