Ontology highlight
ABSTRACT:
SUBMITTER: Hoffmeister H
PROVIDER: S-EPMC10112965 | biostudies-literature | 2023 Apr
REPOSITORIES: biostudies-literature
Hoffmeister Helen H Holzinger Simon S Dürr Marie-Sofie MS Bruckmann Astrid A Schindler Susanne S Gröbner-Ferreira Regina R Depping Reinhard R Längst Gernot G
Journal of cell science 20230406 7
Chromatin remodeling enzymes form large multiprotein complexes that play central roles in regulating access to the genome. Here, we characterize the nuclear import of the human CHD4 protein. We show that CHD4 enters the nucleus by means of several importin-α proteins (1, 5, 6 and 7), but independently of importin β1. Importin α1 directly interacts with a monopartite 'KRKR'-motif in the N-terminus of CHD4 (amino acids 304-307). However, alanine mutagenesis of this motif only leads to an ∼50% redu ...[more]