TY - JOUR
T1 - An early gene of the Chlorella virus PBCV-1 encodes a functional aspartate transcarbamylase
AU - Landstein, Dorit
AU - Mincberg, Michal
AU - Arad, Shoshana
AU - Tal, Jacov
N1 - Funding Information:
We thank James Van Etten for introducing us to the fascinating field of algal viruses, and for his generous support that included virus and algae, protocols and advice. We also thank Yacob Weinstein for his advice throughout this work, Yu Li for correcting a 2 nucleotide mistake in our ATCase sequence, and James Van Etten and Allan Mehler for commenting on the manuscript. This study was supported by the Israel Ministry of Science and Technology.
PY - 1996/7/1
Y1 - 1996/7/1
N2 - PBCV-1 belongs to a family of large viruses that replicate in the exsymbiont green algae Chlorella strain NC64A. The viral, 330-kb DNA genome encodes a relatively large number of functionally active proteins including restriction and modification enzymes, DNA polymerase, glycosylation, and cell wall degrading enzymes. Sequencing of the viral DNA, now in progress, revealed many major open reading frames (ORF), which resemble known genes in sequence data bases and which have not previously been found in viral genomes. Here we report on the identification and characterization of one such gene, aspartate transcarbamylase (ATCase), an enzyme that catalyzes the committing step in the de novo biosynthetic pathway of pyrimidines. The cloned gene is highly homologous to a variety of plant ATCases and includes the typical ATCase catalytic motif. When cloned into the pGEX-2T expression vector, a fusion protein with ATCase activity could be demonstrated and distinguished from the host ATCase activity. The viral enzyme is expressed early and transiently in the infection. To our knowledge, this is the first virus known to encode and express its own de novo nucleotide precursors' synthetic enzymes.
AB - PBCV-1 belongs to a family of large viruses that replicate in the exsymbiont green algae Chlorella strain NC64A. The viral, 330-kb DNA genome encodes a relatively large number of functionally active proteins including restriction and modification enzymes, DNA polymerase, glycosylation, and cell wall degrading enzymes. Sequencing of the viral DNA, now in progress, revealed many major open reading frames (ORF), which resemble known genes in sequence data bases and which have not previously been found in viral genomes. Here we report on the identification and characterization of one such gene, aspartate transcarbamylase (ATCase), an enzyme that catalyzes the committing step in the de novo biosynthetic pathway of pyrimidines. The cloned gene is highly homologous to a variety of plant ATCases and includes the typical ATCase catalytic motif. When cloned into the pGEX-2T expression vector, a fusion protein with ATCase activity could be demonstrated and distinguished from the host ATCase activity. The viral enzyme is expressed early and transiently in the infection. To our knowledge, this is the first virus known to encode and express its own de novo nucleotide precursors' synthetic enzymes.
UR - http://www.scopus.com/inward/record.url?scp=0030199198&partnerID=8YFLogxK
U2 - 10.1006/viro.1996.0361
DO - 10.1006/viro.1996.0361
M3 - Article
AN - SCOPUS:0030199198
SN - 0042-6822
VL - 221
SP - 151
EP - 158
JO - Virology
JF - Virology
IS - 1
ER -