LOCUS GO515252 463 bp mRNA linear EST 14-APR-2009
DEFINITION Mdrtb1020L22.g1 Apple_EST_Mdrtb Malus domestica cDNA 5' similar to
pir|T00044 vacuolar sorting receptor protein homolog PV72 -
cucurbit dbj|BAA25079.1| PV72 [Cucurbita cv. Kurokawa Amakuri],
mRNA sequence.
ACCESSION GO515252
VERSION GO515252.1
DBLINK BioSample: SAMN00167513
KEYWORDS EST.
SOURCE Malus domestica (apple)
ORGANISM Malus domestica
Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
Spermatophyta; Magnoliopsida; eudicotyledons; Gunneridae;
Pentapetalae; rosids; fabids; Rosales; Rosaceae; Amygdaloideae;
Maleae; Malus.
REFERENCE 1 (bases 1 to 463)
AUTHORS Korban,S., Vodkin,L., Liu,L., Gasic,K., Gonzales,O., Hernandez,A.,
Aldwinckle,H., Malnoy,M., Carroll,N., Goldsbrough,P., Orvis,K.,
Clifton,S., Pape,D., Marra,M., Hillier,L., Martin,J., Wylie,T.,
Dante,M., Theising,B., Bowers,Y., Gibbons,M., Ritter,E., Ronko,I.,
Tsagareishvili,R., Kennedy,S., Waterston,R. and Wilson,R.
TITLE Apple Functional Genomics grant - NSF 0321702
JOURNAL Unpublished
COMMENT Contact: Schuyler S. Korban
Apple Functional Genomics grant - NSF 0321702
Washington University School of Medicine
4444 Forest Park Parkway, Box 8501, St. Louis, MO 63108, USA
Tel: 314 286 1800
Fax: 314 286 1810
Email: submissions@watson.wustl.edu
Library material provided by S.Korban/G. Fazio Library constructed
by K. Gasic/S. Korban Library sequenced by Washington University
Genome Sequencing Center
This trace has been recalled with phred
original value before phred recall for SL was 101
original value before phred recall for SR was 869
Seq primer: -40UP.
FEATURES Location/Qualifiers
source 1..463
/organism="Malus domestica"
/mol_type="mRNA"
/cultivar="M.111 rootstock"
/db_xref="taxon:3750"
/tissue_type="Root"
/clone_lib="SAMN00167513 Apple_EST_Mdrtb"
/dev_stage="young root"
/lab_host="DH10B ampicillin resistant"
/note="Vector: pBluescript II SK (+); Site_1: Not I;
Site_2: EcoRI; Total RNA was extracted separately from
whole root using the 'pine tree' method. Poly(A)+mRNA was
isolated twice from total RNA from each stage using the
Oligotex Direct mRNA kit (Qiagen). mRNA was reverse
transcribed into double stranded cDNA using a modified
oligo18(dT) primer with an identifying tag sequence. [Tag
identification when sequencing from 5' end: insert
18(A)TCGTG] Double stranded cDNAs were size selected (more
than 450 bp), adaptored with EcoRI adapters at both ends
and then digested with NotI. The cDNAs were then
directionally cloned into EcoR1-NotI digested pBS II SK(+)
phagemid vector(Stratagene). The total number of white
colony forming units (cfu) was 7.4 x 10^6 cfu (colony
forming units). The background of empty clones was less
than 3%. Inserts ranged from 0.5kb to 3kb, as determined
by PCR."
BASE COUNT 126 a 82 c 147 g 108 t
ORIGIN
1 ttgctgtcgc aaatgcttgc agttgtccac caggattcaa gggtgatgga gagaaaacat
61 gtgaagatgt tgatgagtgc aaggagaaaa cgtcttgcca atgttcacaa tgcaaatgca
121 agaatacttg gggaagttac gagtgcagtt gcggtggcgg tttactgtac atgcgagaaa
181 atgatgcatg tataggtaaa aacggaagtg gttctgggtc tagctggggc ctaatttggg
241 ttatcattct ctgcttgggt gctgtcggag ttgggggctt cgcagtttac aagtaccgaa
301 tccggagata catggattcg gagatccggg caatcatggc gcagtacatg ccgttggatg
361 ggggaggaga agttcccagc cacgtcgccc gcggggatat ctgaaaccgg cggagagacg
421 tattcataaa acataagatg ctgtccgaga gaaaagggaa gac
//