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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 2004 Nov 23;101(47):16707. doi: 10.1073/pnas.0407769101

Correction

PMCID: PMC534544

PHYSIOLOGY. For the article “Transforming growth factor β-induced cell cycle arrest of human hematopoietic cells requires p57KIP2 up-regulation,” by Joseph M. Scandura, Piernicola Boccuni, Joan Massagué, and Stephen D. Nimer, which appeared in issue 42, October 19, 2004, of Proc. Natl. Acad. Sci. USA (101, 15231–15236; first published October 11, 2004; 10.1073/pnas.0406771101), Fig. 3A should have been published in color. The corrected figure and its legend appear below.

Fig. 3.

Fig. 3.

TGFβ induces monoallelic up-regulation of p57 but does not regulate other genes in the imprinted region of chromosome 11p15.5. (A) The genomic organization of a 1-Mb imprinted cluster of genes on chromosome 11p15.5 is shown. Maternally and paternally imprinted genes are represented as pink or blue-filled pentagons, respectively. Nonimprinted genes within the region are shown in black, and those for which the imprinting status is unknown are filled with white. The brackets correspond to the two clusters of genes that are coordinately imprinted and are under the control of independent regulatory elements. (B) The PAPA repeat region was amplified from two individual units of cord blood by using genomic DNA and cDNA made from CB-CD34 cells stimulated with TGFβ for 4 h as templates. Heteroduplexes are seen for the amplified genomic fragments but not when the cDNA is amplified. The doublet seen using genomic DNA but not with the cDNA is due to different allele lengths. (C) p57 mRNA, but not that of other imprinted genes on chromosome 11p15.5, is rapidly up-regulated by TGFβ in CB-CD34. The average signal for the various probe sets is shown normalized to the expression before stimulation with TGFβ.(D) Quantitative RT-PCR analysis of PHLDA2, KCNQ1, IGF2, and CDKN1c (p57) gene expression before and 4 h after exposure of CB-CD34 to TGFβ. Expression of the indicated mRNA is reported relative to the expression of the hypoxanthine phosphoribosyltransferase reference transcript. All error bars represent the standard errors of measurements from three to four independent experiments.


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