TY - JOUR
T1 - A novel imprinted gene, HYMAI, is located within an imprinted domain on human chromosome 6 containing ZAC
AU - Arima, Takahiro
AU - Drewell, Robert A.
AU - Oshimura, Mitsuo
AU - Wake, Norio
AU - Surani, M. Azim
N1 - Funding Information:
We thank Sheila C. Barton and Kathy J. Hilton for technical assistance and all members of the laboratory for their support and valuable suggestions, in particular, R. John, M. Saitou, and I. Szeto for assistance in preparing the manuscript. This work was supported by a Newton Trust grant (T.A.). R.A.D. was funded by a Wellcome Trust Prize Studentship and Fellowship.
PY - 2000/8/1
Y1 - 2000/8/1
N2 - Transient neonatal diabetes mellitus (TNDM) is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal insulin secretion. This disease is associated with paternal uniparental disomy or paternal duplication of chromosome 6, suggesting that the causative gene(s) for TNDM is imprinted. Recently, Gardner et al. (1999, J. Med. Genet. 36: 192-196) proposed that a candidate gene for TNDM lies within chromosome 6q24.1-q24.3. To find human imprinted genes, we performed a database search for EST sequences that mapped to this region, followed by RT-PCR analysis using monochromosomal hybrid cells with a human chromosome 6 of defined parental origin. Here we report the identification of a novel imprinted gene, HYMAI. This gene exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island and is expressed only from the paternal chromosome. A previously characterized imprinted gene, ZAC/LOT1, is located 70 kb downstream of HYMAI and is also expressed only from the paternal allele. In the pancreas, both genes are moderately expressed. HYMAI and ZAC/LOT1 are therefore candidate genes involved in TNDM. Furthermore, the human chromosome 6q24 region is syntenic to mouse chromosome 10 and represents a novel imprinted domain. (C) 2000 Academic Press.
AB - Transient neonatal diabetes mellitus (TNDM) is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal insulin secretion. This disease is associated with paternal uniparental disomy or paternal duplication of chromosome 6, suggesting that the causative gene(s) for TNDM is imprinted. Recently, Gardner et al. (1999, J. Med. Genet. 36: 192-196) proposed that a candidate gene for TNDM lies within chromosome 6q24.1-q24.3. To find human imprinted genes, we performed a database search for EST sequences that mapped to this region, followed by RT-PCR analysis using monochromosomal hybrid cells with a human chromosome 6 of defined parental origin. Here we report the identification of a novel imprinted gene, HYMAI. This gene exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island and is expressed only from the paternal chromosome. A previously characterized imprinted gene, ZAC/LOT1, is located 70 kb downstream of HYMAI and is also expressed only from the paternal allele. In the pancreas, both genes are moderately expressed. HYMAI and ZAC/LOT1 are therefore candidate genes involved in TNDM. Furthermore, the human chromosome 6q24 region is syntenic to mouse chromosome 10 and represents a novel imprinted domain. (C) 2000 Academic Press.
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U2 - 10.1006/geno.2000.6266
DO - 10.1006/geno.2000.6266
M3 - Article
C2 - 10936046
AN - SCOPUS:0034253796
SN - 0888-7543
VL - 67
SP - 248
EP - 255
JO - Genomics
JF - Genomics
IS - 3
ER -