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细胞核中的HIV-1 Nef蛋白通过过氧化物酶体增殖物激活受体影响脂肪生成以及病毒转录。

HIV-1 Nef protein in the nucleus influences adipogenesis as well as viral transcription through the peroxisome proliferator-activated receptors.

作者信息

Otake Kaori, Omoto Shinya, Yamamoto Takuya, Okuyama Harumi, Okada Hidechika, Okada Noriko, Kawai Masahiro, Saksena Nitin K, Fujii Yoichi R

机构信息

Nagoya University Hospital, Japan.

出版信息

AIDS. 2004 Jan 23;18(2):189-98. doi: 10.1097/00002030-200401230-00007.

Abstract

BACKGROUND

Although the HIV-1 Nef protein (27 kDa) localizes primarily in cytoplasm, there is considerable evidence suggesting its occasional localization in the nucleus. Nef is known to play an important role in transcriptional events and viral replication, but the actual target of Nef in the nucleus remains to be identified.

OBJECTIVE

To examine the functional roles of Nef in the nucleus and its possible interactions with other unknown factors in the nucleus.

METHODS

High-density microarray analysis was used to screen directly the unique functions of Nef on host gene transcription. The nuclear localization of Nef and its effects on the expression of peroxisome proliferator-activated receptors (PPAR) was examined using PPAR promoter/reporter assay and immunoblotting. A long terminal repeat/reporter assay was used to investigated the effects of Nef and PPAR on viral transcription.

RESULTS

Nef in the nucleus suppressed PPAR gamma expression and reduced fatty acid levels in human T and macrophage cell lines. Expression of Nef or PPAR suppressed viral replication; the effect of PPAR gamma or retinoid X receptor-alpha on viral replication were reduced by coexpression of Nef in MT(-)4 T cells.

CONCLUSION

Nef may be involved in both viral replication and the wasting syndrome associated with AIDS.

摘要

背景

尽管HIV-1 Nef蛋白(27 kDa)主要定位于细胞质,但有大量证据表明其偶尔也定位于细胞核。已知Nef在转录事件和病毒复制中起重要作用,但Nef在细胞核中的实际靶点仍有待确定。

目的

研究Nef在细胞核中的功能作用及其与细胞核中其他未知因子的可能相互作用。

方法

采用高密度微阵列分析直接筛选Nef对宿主基因转录的独特功能。使用PPAR启动子/报告基因检测和免疫印迹法检测Nef的核定位及其对过氧化物酶体增殖物激活受体(PPAR)表达的影响。使用长末端重复序列/报告基因检测法研究Nef和PPAR对病毒转录的影响。

结果

细胞核中的Nef抑制人T细胞和巨噬细胞系中PPARγ的表达并降低脂肪酸水平。Nef或PPAR的表达抑制病毒复制;在MT(-)4 T细胞中共表达Nef可降低PPARγ或视黄酸X受体α对病毒复制的影响。

结论

Nef可能参与病毒复制以及与艾滋病相关的消瘦综合征。

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