TY - JOUR
T1 - Structure and expression of the mouse L23mrp gene downstream of the imprinted H19 gene
T2 - Biallelic expression and lack of interaction with the H19 enhancers
AU - Zubair, Mohamad
AU - Hilton, Kathy
AU - Saam, Jennifer R.
AU - Surani, M. Azim
AU - Tilghman, Shirley M.
AU - Sasaki, Hiroyuki
N1 - Funding Information:
We gratefully acknowledge Nao Aoki and Hiroyasu Furuumi for technical assistance; Amy T. Hark for help in experiments on the deletion mice; Kazuhito Mizuki, Hideki Sumimoto, and Tetsuyuki Kitamoto for DNA libraries; Nobuo Takagi and Toshihiko Shiroishi for JF1 mice; Tsuyoshi Koide for a cosmid clone; Miho Matsuda for HeLa cell RNA; Dongchon Kang, Yusaku Nakabeppu, and Katsu-yoshi Mihara for discussion; Akiko Iwaki for comments on the manuscript; and Yasuyuki Fukumaki for encouragement. The work was supported by grants from the International Human Frontier Science Program Organization (RG-516/94 M), the Ministry of Education, Science, Sports and Culture of Japan, and the National Institute of General Medical Sciences.
PY - 1997
Y1 - 1997
N2 - The human L23 (mitochondrial)-related protein gene, located 40 kb downstream of the imprinted H19 gene, is biallelically expressed. We have cloned and characterized its mouse homolog, L23mrp, which maps to the conserved syntenic region on mouse chromosome 7. The promoter of L23mrp is a CpG island that is transcribed ubiquitously, but at different levels, in different fetal tissues. Allele-specific expression analysis revealed that both parental alleles are equally active. Since the enhancers located between H19 and L23mrp had been shown to be involved in the imprinted expression of Ins-2, Igf-2, and H19, we asked whether they also influence L23mrp. Analysis of mice with a targeted deletion of the enhancers demonstrated that they were not disrupted in the expression of L23mrp. These findings indicate that L23mrp is functionally insulated from the Ins-2/Igf-2/H19 domain in terms of both imprinting and enhancer action.
AB - The human L23 (mitochondrial)-related protein gene, located 40 kb downstream of the imprinted H19 gene, is biallelically expressed. We have cloned and characterized its mouse homolog, L23mrp, which maps to the conserved syntenic region on mouse chromosome 7. The promoter of L23mrp is a CpG island that is transcribed ubiquitously, but at different levels, in different fetal tissues. Allele-specific expression analysis revealed that both parental alleles are equally active. Since the enhancers located between H19 and L23mrp had been shown to be involved in the imprinted expression of Ins-2, Igf-2, and H19, we asked whether they also influence L23mrp. Analysis of mice with a targeted deletion of the enhancers demonstrated that they were not disrupted in the expression of L23mrp. These findings indicate that L23mrp is functionally insulated from the Ins-2/Igf-2/H19 domain in terms of both imprinting and enhancer action.
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U2 - 10.1006/geno.1997.4961
DO - 10.1006/geno.1997.4961
M3 - Article
C2 - 9344651
AN - SCOPUS:0030671271
SN - 0888-7543
VL - 45
SP - 290
EP - 296
JO - Genomics
JF - Genomics
IS - 2
ER -