Harris et al. Figure 1
FIGURE 1
A schematic of local nucleotide sequence alignments for
ER DBD exon 2 and exon 3 nucleotides ranging from (898 bp to 1116 bp)
of the ER cDNA (GENBANK locus HSERR) vs Vitelligenin A1 (GENBANK locus
XLVITA15) nucleotides ranging from (-428 to -278) upstream from the
Vitelligenin A1 gene transcription start site.
The nucleotide
sequence of VITA1 showing maximal subsequence alignment with ER DBD from
1a above is shown. The EREs of VITA1 are in bold type with the DNA
major groove ERE halfsites underlined. Nucleotide base pair matches are
starred. Vertical lines indicate purine or pyrimidine conserved
transitions. Below the ER DBD cDNA sequence is the corresponding amino
acid sequence in Dayhoff (17) one-letter code with the amino acids
numbered as in the human ER (18). The DNA recognition helix is
underlined.
The maximally similar nucleotide subsequence of the
same VITA1 sequence (-428 to -278) as above vs the ER cDNA (954 bp to
1005 bp) encoding the ER DBD DNA recognition helix is shown.
The
maximally similar nucleotide subsequence of the same VITA1 sequence
(-428 to -278) as above vs the ER cDNA (964 to 1023) which spans the
splice junction site of ER DBD exon 2 and exon 3 encoding the ER DNA
recognition helix of exon 2 and a beta strand of exon 3 is shown.
The maximally similar nucleotide subsequence of the same VITA1 sequence
(-428 to -278) as above vs the ER cDNA (1120 to 1206) of exon 4 which
encodes a predicted alpha helix is shown.