N. Jayawardene et Cd. Riggs, MOLECULAR-CLONING, SEQUENCE-ANALYSIS AND DIFFERENTIAL EXPRESSION OF AN INTRON-CONTAINING GENE ENCODING TOMATO HISTONE H1, European journal of biochemistry, 223(2), 1994, pp. 693-699
A tomato genomic clone has been identified which encodes histone H1. T
he deduced polypeptide is 287 amino acids in length, and exhibits the
tripartite organization typical of histones H1. The central globular d
omain is highly similar to those regions from other H1 molecules, and
the carboxyl-terminal domain contains a repeating hexapeptide motif, v
ariants of which are conserved among H1 molecules. RNA gel blotting re
vealed that histone H1 mRNA is expressed at higher levels in organs wh
ich contain meristematic tissue and/or which have a high proportion of
actively cycling cells. DNA gel blotting and dot-blot hybridization s
tudies revealed that histone H1 in tomato is encoded by a small gene f
amily. By employing the polymerase chain reaction on genomic DNA and o
n cDNA, it was determined that the gene is interrupted by an intron. T
he location and approximate length of the intron are conserved in both
the tomato and Arabidopsis genes, with the intron separating the 'nos
e' region (encoded by exon 1) from the central globular domain (exon 2
). The promoter region was found to contain several conserved sequence
motifs which likely participate in the regulation of the gene.