TY - JOUR
T1 - A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer
AU - Mancini-DiNardo, Debora
AU - Steele, Scott J.S.
AU - Ingram, Robert S.
AU - Tilghman, Shirley M.
N1 - Funding Information:
We would like to thank B. K. Jones for her gift of RNAs used for the RNase protection analysis and advice on the DNase I hypersensitivity analysis; A. West and C. Schoenherr for advice on the enhancer blocking assays; M.A. Cleary and J.V. Schmidt for advice and reagents; and members of the Tilghman lab for their helpful comments and suggestions on the manuscript. D.M.D. is supported by the Cancer Research Fund of the Damon Runyon Foundation Fellowship, DRG no. 1675. S.J.S.S. is supported by the New Jersey Commission on Cancer Research. This work was supported by a grant from the NIH. S.M.T. was an investigator of the Howard Hughes Medical Institute.
PY - 2003/2/1
Y1 - 2003/2/1
N2 - The imprinted gene cluster on mouse distal chromosome 7 contains a differentially methylated CpG island that maps within the Kcnq1 gene that has been shown to be required for the imprinting of multiple genes. To evaluate models for how this imprinting control region (ICR) regulates imprinting, we have characterized it structurally and functionally. We show that the region contains a promoter for a paternally expressed anti-sense transcript, Kcnq1ot1, and we define the extent of the minimal promoter. We describe three paternal-specific nuclease hypersensitive sites immediately upstream from the start site and show that they are required for full promoter activity. The expression of Kcnq1ot1 during pre- and postnatal development is compared to that of other imprinted genes in its vicinity, Cdnkn1c and Kcnq1. The lack of coordination in their expression tends to rule out an enhancer competition model for the action of the ICR in imprinting control. Using a stable transfection assay we show that the region contains a position-independent and orientation-independent silencer. We propose, on the basis of these findings, that the Kcnq1 ICR functions as a silencer on the paternal chromosome to effect the repression of neighboring genes.
AB - The imprinted gene cluster on mouse distal chromosome 7 contains a differentially methylated CpG island that maps within the Kcnq1 gene that has been shown to be required for the imprinting of multiple genes. To evaluate models for how this imprinting control region (ICR) regulates imprinting, we have characterized it structurally and functionally. We show that the region contains a promoter for a paternally expressed anti-sense transcript, Kcnq1ot1, and we define the extent of the minimal promoter. We describe three paternal-specific nuclease hypersensitive sites immediately upstream from the start site and show that they are required for full promoter activity. The expression of Kcnq1ot1 during pre- and postnatal development is compared to that of other imprinted genes in its vicinity, Cdnkn1c and Kcnq1. The lack of coordination in their expression tends to rule out an enhancer competition model for the action of the ICR in imprinting control. Using a stable transfection assay we show that the region contains a position-independent and orientation-independent silencer. We propose, on the basis of these findings, that the Kcnq1 ICR functions as a silencer on the paternal chromosome to effect the repression of neighboring genes.
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U2 - 10.1093/hmg/ddg024
DO - 10.1093/hmg/ddg024
M3 - Review article
C2 - 12554682
AN - SCOPUS:0037321187
SN - 0964-6906
VL - 12
SP - 283
EP - 294
JO - Human molecular genetics
JF - Human molecular genetics
IS - 3
ER -