Beta-tubulin, one of the cytoskeletal proteins, has been highly conserved throughout the evolution of eukaryotes. Degenerate
PCR and inverse PCR (iPCR) were used to isolate the full-length beta-tubulin gene and its 5′ and 3′-flanking regions (2799bp)
from the marine red alga
Porphyra yezoensis. This gene, designated as
TubB1, is devoid of introns. The canonical cis-acting elements such as TATA box, CAAT box and polyA signal AAUAAA are not found
in flanking sequences, but another putative polyA signal CAYTG is found downstream of the stop codon. Comparison of the deduced
458 amino acid sequences shows higher similarity to the Protoflorideophycidae
Cyanidioschyzon merolae (82%) than to the red alga
Chondrus crispus (79%). Codon bias indicates strong expression of
TubB1. Phylogenetic analysis suggests that the beta-tubulin of
P. yezoensis and
C. merola go together with fungi and not with green plants. These nucleotide sequence data have been deposited in the DDB/EMBL/Genbank
databases under the accession number AY221630.
Keywords beta-tubulin - intronless - inverse PCR -
Porphyra yezoensis
- Rhodophyta - sequence analysis