Basic amino acid residues located in the N-terminal region of BEND3 are essential for its nuclear localization
Creators
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.2015.01.029Additional 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.