Summary
Normal quiescent lymphocytes regulate their ribosome content by selectively degrading newly synthesized 18S ribosomal RNA. Unlike actively dividing HeLa cells, lymphocytes retain 18 S ribosomal RNA in the nucleus after synthesis instead of immediately transporting it to the cytoplasm. Subcellular fractionation of the highly differentiated human neoplastic lymphocyte RPMI-8226 reveals that this cell line also retains 18 S ribosomal RNA in the nucleus, a trait not displayed by the less differentiated human lymphoblastoid cell line RPMI-4265. These observations suggest that neoplastic cells can be phenotypically characterized by their ribosomal RNA processing patterns.
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Bynum, J.W., Volkin, E. Nuclear retention of 18S ribosomal RNA by human myeloma cells. Cell Tissue Res. 197, 347–351 (1979). https://doi.org/10.1007/BF00233925
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DOI: https://doi.org/10.1007/BF00233925