Human CKAP2L shows a cell cycle‐dependent expression pattern and exhibits microtubule‐stabilizing properties

Author:

Kwon Hyerim1,Joh Jonathan Y.2,Hong Kyung U.3ORCID

Affiliation:

1. School of Medicine Sungkyunkwan University Suwon Korea

2. Department of Pharmacology & Toxicology University of Louisville School of Medicine KY USA

3. College of Pharmacy and Health Sciences Western New England University Springfield MA USA

Abstract

Cytoskeleton‐associated protein 2‐like (CKAP2L) is a paralogue of cytoskeleton‐associated protein 2 (CKAP2). We characterized the expression pattern, subcellular localization, and microtubule‐stabilizing properties of human CKAP2L. The levels of both CKAP2L transcript and protein were cell cycle phase‐dependent, peaking during the G2/M phase and relatively high in certain human tissues, including testis, intestine, and spleen. CKAP2L protein was detectable in all human cancer cell lines we tested. CKAP2L localized to the mitotic spindle apparatus during mitosis, as reported previously. During interphase, however, CKAP2L localized mainly to the nucleus. Ectopic overexpression of CKAP2L resulted in ‘microtubule bundling’, and, consequently, an elevated CKAP2L level led to prolonged mitosis. These findings support the mitotic role of CKAP2L during the human cell cycle.

Publisher

Wiley

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