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Correction| January 10 2011

ERK1/2 MAP kinases promote cell cycle entry by rapid, kinase-independent disruption of retinoblastoma–lamin A complexes

Javier Rodríguez,

Javier Rodríguez

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Fernando Calvo,

Fernando Calvo

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José M. González,

José M. González

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Berta Casar,

Berta Casar

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Vicente Andrés,

Vicente Andrés

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Piero Crespo

Piero Crespo

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Author and Article Information

Javier Rodríguez

Fernando Calvo

José M. González

Berta Casar

Vicente Andrés

Piero Crespo

Online ISSN: 1540-8140

Print ISSN: 0021-9525

© 2011 Rodríguez et al.

2011

J Cell Biol (2011) 192 (1): 201.

https://doi.org/10.1083/jcb.20100406720101203c

Vol. 191 No. 5, November 29, 2010. Pages 967–979.

The authors have detected a labeling error in Fig. 3 A. The corrected panel appears below.

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© 2011 Rodríguez et al.

2011

Figure 3.

Figure 3. ERK2 does not affect other lamin A and Rb interactions. (A) ERK2 does not affect LAP2α–Rb interaction. NIH3T3 cells were transfected with 1 μg each of vector (−), HA-ERK2-NLS-wt (wt), and HA-ERK2-DK (DK), grown until confluence, and kept in 0.5% CS for 18 h. Cellular lysates were immunoprecipitated with an antibody against LAP2α or with preimmune serum (PI), and immunoprecipitates (IP) and total lysates (TL) were probed for the indicated proteins (α protein of interest).

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ERK2 does not affect other lamin A and Rb interactions. (A) ERK2 does not affect LAP2α–Rb interaction. NIH3T3 cells were transfected with 1 μg each of vector (−), HA-ERK2-NLS-wt (wt), and HA-ERK2-DK (DK), grown until confluence, and kept in 0.5% CS for 18 h. Cellular lysates were immunoprecipitated with an antibody against LAP2α or with preimmune serum (PI), and immunoprecipitates (IP) and total lysates (TL) were probed for the indicated proteins (α protein of interest).