M. Feldbrugge et al., THE TRANSCRIPTIONAL REGULATOR CPRF1 - EXPRESSION ANALYSIS AND GENE STRUCTURE, MGG. Molecular & general genetics, 251(6), 1996, pp. 619-627
Many eukaryotic DNA-binding proteins share a conserved amino acid sequ
ence known as the basic region leucine zipper (bZIP) domain. bZIP prot
eins recognise DNA, upon dimerization, in a sequence-specific manner.
The Common Plant Regulatory Factor 1 (CPRF1) is a bZIP transcription f
actor from parsley (Petroselinum crispum), which recognises defined el
ements containing ACGT cores. CPRF1 genomic DNA was cloned and the gen
e was sequenced. Analysis of the sequence data revealed the existence
of 12 exons and 11 introns within a stretch of about 9 kb. A second RN
A species hybridising to CPRF1 probes was identified as an alternative
ly spliced, additional CPRF1 transcript containing intron 8. This poly
adenylated RNA species showed accumulation characteristics very simila
r to those of the CPRF1 mRNA. CPRF1 specifically binds an ACGT-contain
ing element which is located within the composite regulatory unit that
is necessary and sufficient for light activation of the parsley chalc
one synthase (CHS) minimal promoter. Expression studies at the mRNA le
vel demonstrated that CPRF1 mRNA is present in all organs of light-gro
wn plants in which CHS mRNA expression is detectable, and light-depend
ent CHS mRNA accumulation was shown to be blocked by cycloheximide. Th
erefore, translation of a protein factor, possibly CPRF1, may be a pre
requisite for CHS promoter activation.