Cyclin B 5' regulatory region
LOCUS Rr_SPCYCB 538 bp DNA INV 14-MAY-1998
DEFINITION Strongylocentrotus purpuratus cyclin B gene, 5' regulatory region
DBSOURCE GENBANK: name S80441, accession S80441
KEYWORDS .
SOURCE purple urchin.
ORGANISM Strongylocentrotus purpuratus
Eukaryotae; mitochondrial eukaryotes; Metazoa; Echinodermata;
Echinozoa; Echinoidea; Euechinoidea; Echinacea; Echinoida;
Strongylocentrotidae; Strongylocentrotus.
REFERENCE 1 (bases 1 to 538)
AUTHORS Thatcher,J.D., McBride,B. and Katula,K.S.
TITLE Promoter binding factors regulating cyclin B transcription in the
sea urchin embryo
JOURNAL DNA Cell Biol. 14 (10), 869-881 (1995)
MEDLINE 96027756
COMMENTS DNase I footprinting of the cyclin B upstream region revealed eight
binding regions within 435 bp of the start of transcription; seven
of these sites are within 215 bp. Found within these regions were
consensus sequences for two CCAAT boxes, TATA and E-boxes, and sequences
with some similarity to E2F and octamer binding motifs. Upstream
sequences were functionally defined by generating cyclin B-CAT fusion
genes, containing deletions and base specific mutations, and testing
for relative levels of expression by gene transfer. Both CCAAT boxes
were found to be essential for maximal levels of expression. A third
binding site (PR7) with no recognizable consensus sequence was also
found to act as a positive element. Experiments show that protein
binding to the E2F-like sequences may act to reduce expression.
Sequence comparisons and methylation interference data indicate
that the likely protein binding the CCAAT sequences is the characterized
CCAAT-binding protein CP1. The results indicate that cyclin B is subject
to positive and negative regulation, involving multiple factors that
bind between -200 and -90 bp from the start of transcription [1].
FEATURES Location/Qualifiers
source 1..538
/organism="Strongylocentrotus purpuratus"
/db_xref="taxon:7668"
mRNA 442..
protein_bind 7..40
/citation=[1]
/evidence=DNaseI footprinting
/site="PR8"
/note="octamer element"
protein_bind 224..247
/citation=[1]
/evidence=DNaseI footprinting
/site="PR7"
protein_bind 272..289
/citation=[1]
/site="PR6"
/evidence=DNaseI footprinting
/note="CCAAT box"
protein_bind 309..323
/citation=[1]
/site="PR4"
/evidence=DNaseI footprinting
/note="CCAAT box"
protein_bind 326..337
/citation=[1]
/site="PR3"
/evidence=DNaseI footprinting
/note="E2F"
protein_bind 348..400
/citation=[1]
/site="PR2"
/evidence=DNaseI footprinting
/note="E2F and two E-boxes"
protein_bind 408..427
/citation=[1]
/site="PR1"
/evidence=DNaseI footprinting
/note="TATA"
protein_bind 435..477
/citation=[1]
/site="PR0"
/evidence=DNaseI footprinting
/note="E-box and transcription start"
TATA_signal 414..417
ORIGIN
1 tttgttttaa aaatatgcat acaatttaaa tatgttatta caccggtcgc tttggcactg
61 ctgaaaaagt actttaattt cttttctctc tctcattgta tggatcaact atgtgactaa
121 tttacattcc tagctacatg tatagcacca gcaggtgttt gacgagtgga tacctccatc
181 gcgcatacca ccattgaatg ttaccactcc gactcatcaa ggcaagagga acgacctcta
241 ttgatcgcct agcaatgcat cttttacatc accattgacc aatcagcgcc gtgaagtagc
301 gatcaacgga ccaatcaggt tgcccccgcg atattcaagc acggtccgcg acaataacaa
361 aaatcctacg tgcattatcc atatgcgttc attcatttgc acacactgca ctatatattg
421 cgttagctgc ctacacattt gaatccgact cattctgaaa gctgaaaaca actcggacag
481 ttctcatcct agacatcgat aatcgaagaa tttccatact ttgnagtgct aaatcatg