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Correction for Sviderskaya et al., J. Natl. Cancer Inst. 94 (6) 446-454.
JNCI Journal of the National Cancer Institute 2002 94(11):866;
© 2002 by Oxford University Press
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Journal of the National Cancer Institute, Vol. 94, No. 11, 866, June 5, 2002
© 2002 Oxford University Press

CORRESPONDENCE

Erratum:

"p16Ink4a in Melanocyte Senescence and Differentiation" by Sviderskaya et al. [J Natl Cancer Inst 2002;94:446–54 (Issue 6)]. Figure 6Go should have been printed in color. The figure legend and color figure are shown below. The Journal regrets the error.



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  		Fig. 6. Cell morphology and {beta}-galactosidase expression after infection of Ink4a-Arf–/– melanocytes with retroviral vectors containing p16 or Arf complementary DNAs. Melan-Ink4a-1 mouse melanocyte cultures, 12 days after infection, were stained overnight to show activity of acidic {beta}-galactosidase at pH 6.0 (24). A) Control cultures, infected with pBABE-puro only, typically formed quite large clonal colonies that did not stain blue for acidic {beta}-galactosidase. B) Cultures infected with pBABE-puro-p16 formed mostly small colonies or single cells that were generally large and flat. Most cells showed juxtanuclear blue stain for acidic {beta}-galactosidase. Bar = 100 µm. C and D) Cultures infected with pBABE-puro-Arf were generally composed of single, highly pigmented cells that were bipolar or dendritic rather than flat. However, few cells were viable. These cells lacked staining for acidic {beta}-galactosidase, although a faint stain might have been masked by the melanin. Bar = 200 µm in A, C, and D.

 


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