Functional MxA promoter polymorphism associated with subacute sclerosing panencephalitis
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Torisu, H
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Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Torisu, H
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Kusuhara, K
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Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Kusuhara, K
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Kira, R
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Bassuny, WM
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Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Bassuny, WM
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Sakai, Y
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Sanefuji, M
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Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Sanefuji, M
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Takemoto, M
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Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Takemoto, M
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Hara, T
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Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, JapanKyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Hara, T
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[1] Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Higashi Ku, Fukuoka 208128582, Japan
Background: The antivirally active MxA protein is induced by interferon (IFN) alpha/beta and inhibits the replication of single-stranded RNA viruses including measles virus (MV). The authors investigated whether the MxA gene contributed to the development of subacute sclerosing panencephalitis (SSPE) in Japanese individuals. Methods: Single-nucleotide polymorphisms (SNP) in the promoter region of the MxA gene were screened, association studies were performed between two SNP and SSPE, and then a functional difference in the promoter activities of the two SNP was investigated by a dual luciferase reporter assay. Results: Four SNP were found (-88 G/T, -123 C/A, -200 T/C, and -213 G/T), and SSPE patients exhibited a higher frequency of both the -88T allele and the -88TT genotype than controls (p=0.040 and 0.003). The IFN-induced up-regulation of the MxA promoter activity of the sequence with -88T was found to be significantly higher than that with G. Conclusions: MxA promoter -88 G/T SNP may confer host genetic susceptibility to SSPE in Japanese individuals. The finding that homozygotes of the MxA -88T allele with a high MxA-producing capability were more frequently seen in SSPE patients suggests that the MxA protein promotes the establishment of persistent MV infection of neural cells.