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Appl. Environ. Microbiol., 10 1997, 4010-4014, Vol 63, No. 10
LC Cheng, SP Hwang and J Chang
To identify a phytoplankton cell cycle marker detected by a monoclonal
antibody against mammalian proliferating cell nuclear antigen (PCNA) (S.
Lin, J. Chang, and E. J. Carpenter, J. Phycol. 30:449-456, 1994), a PCNA
gene fragment was isolated by reverse transcription-PCR from the marine
unicellular alga Tetraselmis chui Butcher (Prasinophyceae). The gene
fragment was 616 bp in length and contained an open reading frame of 205
amino acids. The deduced amino acid sequence showed 80 and 88% similarity
to human and rice PCNA, respectively. Southern hybridization indicated that
the isolated gene fragment was part of the T. chui genome, with up to three
copies in each haploid nucleus. Northern hybridization was used to detect a
PCNA mRNA with a size of 1.2 kb from an exponentially growing algal
culture. The T. chui gene fragment has been cloned into an expression
vector, and a fusion protein was subsequently generated. Anti-rat PCNA
simultaneously recognized the PCNA fusion protein and a single 33-kDa band
in T.chui total protein extract. Our results indicate that T. chui PCNA is
highly similar to its mammalian counterpart and that anti-rat PCNA is a
good tool for detecting phytoplankton PCNA in general.
Copyright © 1997, American Society for Microbiology
Gene sequence and expression of an analog of proliferating cell nuclear antigen (PCNA) in the alga Tetraselmis chui and detection of the encoded protein with anti-rat PCNA monoclonal antibody
Institute of Marine Biology, Taiwan Ocean University, Keelung, Republic of China.
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