Abstract:
:ADP-ribosylation of HeLa nonhistone proteins was investigated by using [3H]adenosine as an in vivo radioactive label. The aim was to determine basic differences in the patterns of modification of interphase and metaphase nonhistones. Fluorography revealed a relatively small number of modified proteins for isolated metaphase chromosomes. In addition to the core histones, a protein of 116 kDa, which is identified as poly-(ADP-ribose) polymerase, was a primary acceptor of [3H]adenosine. Two-dimensional gels revealed a profound difference in the modification of metaphase and interphase nonhistones. For interphase nuclei, 3H label was distributed among a large number of nonhistone acceptors.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Adolph KW,Song MKdoi
10.1016/0014-5793(85)81174-1subject
Has Abstractpub_date
1985-03-11 00:00:00pages
158-62issue
1eissn
0014-5793issn
1873-3468pii
0014-5793(85)81174-1journal_volume
182pub_type
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