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Correction| September 21 2009

Recruitment of functionally distinct membrane proteins to chromatin mediates nuclear envelope formation in vivo

Daniel J. Anderson,

Daniel J. Anderson

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Jesse D. Vargas,

Jesse D. Vargas

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Joshua P. Hsiao,

Joshua P. Hsiao

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Martin W. Hetzer

Martin W. Hetzer

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Author and Article Information

Daniel J. Anderson , Jesse D. Vargas , Joshua P. Hsiao , Martin W. Hetzer

Online ISSN: 1540-8140

Print ISSN: 0021-9525

© 2009 The Rockefeller University Press

2009

J Cell Biol (2009) 186 (6): 929.

https://doi.org/10.1083/jcb.20090110620090903c

Vol. 186 No. 2, July 27, 2009. Pages 183–191.

The top row of Fig. 4 C was labeled incorrectly, and should appear as “Control”.

The far right column of Fig. S2 B was labeled incorrectly, and should appear as “LMN + TM”.

Corrected images appear below.

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© 2009 The Rockefeller University Press

2009

Figure 4.

Figure 4. (C) Representative images of U2OS cells with Sec61-GFP (green) and H2B-tdTomato (red) compares control cells with cells in which NE formation was accelerated by overexpression of Lap2β, and the distance between chromosome clusters was measured. t = 0 is set at anaphase onset. White lines indicate distances measured in Photoshop extended. Bar, 20 μm.

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(C) Representative images of U2OS cells with Sec61-GFP (green) and H2B-tdTomato (red) compares control cells with cells in which NE formation was accelerated by overexpression of Lap2β, and the distance between chromosome clusters was measured. t = 0 is set at anaphase onset. White lines indicate distances measured in Photoshop extended. Bar, 20 μm.

Figure S2.

Figure S2. (B) Localization of V5-tagged fragments of Lap2β was characterized by immunofluorescence. Bar, 20 μm.

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(B) Localization of V5-tagged fragments of Lap2β was characterized by immunofluorescence. Bar, 20 μm.