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J Virol. 1974 October; 14(4): 715-723
Copyright © 1974 American Society for Microbiology. All Rights Reserved.

Poly(A) Polymerase from Vaccinia Virus-Infected Cells I. Partial Purification and Characterization

Christine Brakel1 and Joseph R. Kates2

a Department of Chemistry, University of Colorado, Boulder, Colorado 80302

ABSTRACT

Poly(A) polymerase activity is induced during vaccinia virus infection of HeLa cells. The enzyme is maximally induced at 3.5 h postinfection. Partial purification frees the preparation of RNase activity and RNA polymerase activity. ATP is the substrate for poly(A) synthesis. A small amount of poly(A) is produced from added adenosine diphosphate due to the production of ATP by an adenylate kinase present in the preparation. The incorporation of ATP into poly(A) is dependent on divalent cations (Mg2+ or Mn2+) and is not inhibited by UTP, CTP, or GTP. Poly(U) stimulates ATP incorporation; poly(A) and poly(C) have little effect on ATP incorporation, and poly(dT) is extremely inhibitory. RNA prepared from HeLa cells and from the partially purified poly(A) polymerase (the enzyme preparation contains endogenous RNA [Brakel and Kates]) stimulates ATP incorporation by poly(A) polymerase which was subjected to DEAE-cellulose chromatography. RNase's, pancreatic and T1, inhibit the production of poly(A). DNase has little effect. Poly(U) is able to stimulate poly(A) production in the presence of T1 RNase.


FOOTNOTES

1 Present Address: University of California at San Francisco, Department of Biochemistry and Biophysics, San Francisco, Calif. 94143.

2 Present Address: State University of New York at Stony Brook, Department of Microbiology, Stony Brook, N.Y. 11790.


J Virol. 1974 October; 14(4): 715-723
Copyright © 1974 American Society for Microbiology. All Rights Reserved.







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Copyright © 1974 by the American Society for Microbiology. All rights reserved.