Published February 20, 2015 | Version v1
Journal article

Basic amino acid residues located in the N-terminal region of BEND3 are essential for its nuclear localization

Description

BEN domain-containing protein 3 (BEND3) has recently been reported to function as a heterochromatin-associated protein in transcriptional repression in the nucleus. BEND3 should have nuclear localization signals (NLSs) to localize to the nucleus in light of its molecular weight, which is higher than that allowed to pass through nuclear pore complexes. We here analyzed the subcellular localization of deletion/site-directed mutants of human BEND3 by an immunofluorescence assay in an attempt to identify the amino acids essential for its nuclear localization. We found that three basic amino acid residues located in the N-terminal region of BEND3 (BEND356–58, KRK) are essential, suggesting that these residues play a role as a functional NLS. These results provide valuable information for progressing research on BEND3. - Highlights: • BEND3 localizes to the nucleus. • The N-terminal 60 amino acids region of BEND3 contains NLS. • Amino acids located between 56 and 58 of BEND3 (KRK) are part of NLS. • KRK motif is highly conserved among BEND3 homologs

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2015.01.029

Additional details

Identifiers

DOI
10.1016/j.bbrc.2015.01.029;
PII
S0006-291X(15)00051-0;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
457
Journal Issue
4
Journal Page Range
p. 589-594
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47028067
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
AMINO ACIDS; CELL NUCLEI; DATA; HETEROCHROMATIN; MOLECULAR WEIGHT; MUTANTS; PROTEINS; SIGNALS; VISIBLE RADIATION
Descriptors DEC
CARBOXYLIC ACIDS; CELL CONSTITUENTS; CHROMATIN; ELECTROMAGNETIC RADIATION; INFORMATION; ORGANIC ACIDS; ORGANIC COMPOUNDS; RADIATIONS

Optional Information

Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.