Molecular characterization of a putative antiretroviral transcriptional factor, OTK18

被引:27
作者
Carlson, KA
Leisman, G
Limoges, J
Pohlman, GD
Horiba, M
Buescher, J
Gendelman, HE
Ikezu, T
机构
[1] Univ Nebraska, Med Ctr, Dept Pathol & Microbiol,Nebraska Med Ctr 985215, Ctr Neurovirol & Neurodegenerat Disorders, Omaha, NE 68198 USA
[2] Univ Nebraska, Med Ctr, Ctr Neurovirol & Neurodegenerat Disorders, Dept Internal Med, Omaha, NE 68198 USA
关键词
D O I
10.4049/jimmunol.172.1.381
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Elucidation of the factors involved in host defense against human immunodeficiency viral infection remains pivotal if viral control may be achieved. Toward these ends, we investigated the function of a putative antiretroviral factor, OTK18, isolated by differential display of mRNA from HIV type 1-infected primary human monocyte-derived macrophages. Molecular and immunohistochemical analyses showed that the OTK18 nucleotide sequence contains 13 adjacent C2H2-type zinc finger motifs, a Kruppel-associated box, and is localized to both cytosol and nucleus. Mutational analyses revealed that both the Kruppel-associated box and zinc finger regions of OTK18 are responsible for the transcriptional suppressive activities of this gene. OTK18 was copiously expressed in macrophages following HIV type I infection and diminished progeny virion production. A mechanism for this antiretroviral activity was by suppression of HIV type I Tat-induced viral long terminal repeat promoter activity. Our findings suggest that one possible function of OTK18 is as a HIV type 1-inducible transcriptional suppresser.
引用
收藏
页码:381 / 391
页数:11
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