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Mol. Cell. Biol., 04 1995, 2051-2062, Vol 15, No. 4
G Houge, B Robaye, TS Eikhom, J Golstein, G Mellgren, BT Gjertsen, M Lanotte and SO Doskeland
Bona fide apoptosis in rat and human leukemia cells, rat thymocytes, and
bovine endothelial cells was accompanied by limited and specific cleavage
of polysome-associated and monosome-associated 28S rRNA, with 18S rRNA
being spared. Specific 28S rRNA cleavage was observed in all instances of
apoptotic death accompanied by internucleosomal DNA fragmentation, with
cleavage of 28S rRNA and of DNA being linked temporally. This indicates
that 28S rRNA fragmentation may be as general a feature of apoptosis as
internucleosomal DNA fragmentation and that concerted specific cleavage of
intra- and extranuclear polynucleotides occurs in apoptosis.
Apoptosis-associated cleavage sites were mapped to the 28S rRNA divergent
domains D2, D6 (endothelial cells), and D8. The D2 cuts occurred in hairpin
loop junctions considered to be buried in the intact ribosome, suggesting
that this rRNA region becomes a target for RNase attack in apoptotic cells.
D8 was cleaved in two exposed UU(U) sequences in bulge loops. Treatment
with agents causing necrotic cell death or aging of cell lysates failed to
produce any detectable limited D2 cleavage but did produce a more
generalized cleavage in the D8 region. Of potential functional interest was
the finding that the primary cuts in D2 exactly flanked a 0.3-kb
hypervariable subdomain (D2c), allowing excision of the latter. The
implication of hypervariable rRNA domains in apoptosis represents the first
association of any functional process with these enigmatic parts of the
ribosomes.
Copyright © 1995, American Society for Microbiology
Fine mapping of 28S rRNA sites specifically cleaved in cells undergoing apoptosis
Department of Anatomy and Cell Biology, University of Bergen, Norway.
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