Structural and functional characterization of herpes simplex virus 1 immediate-early protein infected-cell protein 22.

Abstract:

:Of the five HSV1 immediate-early proteins, infected-cell protein 22 (ICP22), the product of the Us1 gene, is a member whose function is less understood. In order to promote better understanding of the role of ICP22 in viral replication, mutation and fluorescence techniques were used to investigate the biochemical relationship between ICP22's structure and nuclear localization, and the CAT assay was used to analyze the relationship between ICP22's structure and its transcriptional repression. The results of these experiments implied (i) ICP22 is localized to small dense nuclear bodies and is paired with the SC-35 domain in the nucleus, (ii) ICP22 localization in a punctate state requires completion of the main sequence which includes the 1-320th amino acids, (iii) a conservative mutation in the nucleotidylylation site is important for its nuclear localization and transcriptional repression, and (4) despite possessing the same amino acid sequence as the ICP22 carboxyl-terminal, Us1.5 was distinct from ICP22 in location and function.

journal_name

J Biochem

journal_title

Journal of biochemistry

authors

Cun W,Hong M,Liu LD,Dong CH,Luo J,Li QH

doi

10.1093/jb/mvj135

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

67-73

issue

1

eissn

0021-924X

issn

1756-2651

pii

140/1/67

journal_volume

140

pub_type

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