Identification of nuclear localization signals in the human homeoprotein MSX1

Author:

Shibata Akio12,Machida Junichiro13,Yamaguchi Seishi14,Kimura Masashi15,Tatematsu Tadashi12,Miyachi Hitoshi1,Nakayama Atsuo6,Shimozato Kazuo1,Tokita Yoshihito2

Affiliation:

1. Department of Maxillofacial Surgery, Aichi-Gakuin University School of Dentistry, Nagoya, Japan.

2. Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Japan.

3. Department of Oral and Maxillofacial Surgery, Toyota Memorial Hospital, Toyota, Japan.

4. Department of Dentistry and Oral Surgery, Aichi Children’s Health and Medical Center, Obu, Japan.

5. Department of Oral and Maxillofacial Surgery, Ogaki Municipal Hospital, Ogaki, Japan.

6. Department of Embryology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Japan.

Abstract

MSX1 is one of the homeoproteins with the homeodomain (HD) sequence, which regulates proliferation and differentiation of mesenchymal cells. In this study, we investigated the nuclear localization signal (NLS) in the MSX1 HD by deletion and amino acid substitution analyses. The web-based tool NLStradamus predicted 2 putative basic motifs in the N- and C-termini of the MSX1 HD. Green fluorescent protein (GFP) chimera studies revealed that NLS1 (161RKHKTNRKPR170) and NLS2 (216NRRAKAKR223) were independently insufficient for robust nuclear localization. However, they can work cooperatively to promote nuclear localization of MSX1, as was shown by the 2 tandem NLS motifs partially restoring functional NLS, leading to a significant nuclear accumulation of the GFP chimera. These results demonstrate a unique NLS motif in MSX1, which consists of an essential single core motif in helix-I, with weak potency, and an auxiliary subdomain in helix-III, which alone does not have nuclear localization potency. Additionally, other peptide sequences, other than predicted 2 motifs in the spacer, may be necessary for complete nuclear localization in MSX1 HD.

Publisher

Canadian Science Publishing

Subject

Cell Biology,Molecular Biology,Biochemistry

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