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Volume 272, Number 10,
Issue of March 7, 1997
pp. 6677-6684
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Native Recombinant Cyclophilins A, B, and C Degrade DNA
Independently of Peptidylprolyl cis-trans-Isomerase
Activity
POTENTIAL ROLES OF CYCLOPHILINS IN APOPTOSIS
(Received for publication, October 1, 1996)
Jennifer W.
Montague
,
Francis M.
Hughes
Jr.
and
John A.
Cidlowski
From the Department of Biochemistry and Biophysics,
University of North Carolina, Chapel Hill, North Carolina 27599 and
¶ NIEHS, National Institutes of Health, Research Triangle Park,
North Carolina 27709
Previous work in our laboratory (Montague, J.,
Gaido, M., Frye, C., and Cidlowski, J. (1994) J. Biol.
Chem. 269, 18877-18880) has shown that human recombinant
cyclophilins A, B, and C have sequence homology with the apoptotic
nuclease NUC18 and that denatured cyclophilins can degrade DNA. We have
now evaluated the nucleolytic activity of recombinant cyclophilins
under native conditions. We show that nuclease activity inherent to
cyclophilins is distinct from cis-trans-peptidylprolyl
isomerase activity and is similar to that described for apoptotic
nucleases. Cyclophilin nucleolytic activity is stimulated by
Ca2+ and/or Mg2+, with a combination of the two
being optimal for cyclophilins A and B. Mg2+ alone is
sufficient for cyclophilin C nuclease activity. pH optimums are in the
range of pH 7.5-9.5. Cyclophilins can degrade both single-stranded and
double-stranded DNA. Additionally, cyclophilins produce 3 -OH termini
in linear double-stranded substrates, suggesting the cuts produced are
similar to those of apoptotic cells. Cyclophilins also display
endonucleolytic activity, demonstrated by their ability to degrade
supercoiled DNA. In the absence of ions, cyclophilins bind linearized
DNA. When added to nuclei from nonapoptotic cells, cyclophilin C
induces 50-kilobase pair DNA fragmentation but not internucleosomal
fragmentation. Together, these data suggest that cyclophilins are
involved in degradation of the genome during apoptosis.

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Copyright © 1997 by the American Society for Biochemistry and Molecular Biology.
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