Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/31855
Title: Microtubule association of EML proteins and the EML4-ALK variant 3 oncoprotein require an N-terminal trimerization domain.
Authors: Richards, Mark W.
O'Regan, Laura
Roth, D.
Montgomery, Jessica M.
Straube, A.
Fry, Andrew M.
Bayliss, R.
First Published: 5-Mar-2015
Publisher: Portland Press for Biochemical Society
Citation: Biochemical Journal, 2015
Abstract: Proteins of the echinoderm microtubule associated protein-like (EML) family contribute to formation of the mitotic spindle and interphase microtubule (MT) network. EML1-4 consist of WD40 repeats and an N-terminal region containing a putative coiled-coil. Recurrent gene rearrangements in non-small cell lung cancer (NSCLC) fuse EML4 to anaplastic lymphoma kinase (ALK) causing expression of several oncogenic fusion variants. The fusions have constitutive ALK activity due to self-association through the EML4 coiled-coil. We have determined crystal structures of the coiled-coils from EML2 and EML4, which describe the structural basis of both EML self-association and oncogenic EML4-ALK activation. The structures reveal a trimeric oligomerization state directed by a conserved pattern of hydrophobic residues and salt bridges. We show that the trimerization domain (TD) of EML1 is necessary and sufficient for self-association. The TD is also essential for MT binding, however this property requires an adjacent basic region. These observations prompted us to investigate MT association of EML4-ALK and EML1-ABL1 fusions in which variable portions of the EML component are present. Uniquely, EML4-ALK variant 3, which includes the TD and basic region of EML4 but none of the WD40 repeats, was localized to MTs, both when expressed recombinantly and in a patient-derived NSCLC cell line (H2228). This raises the question of whether the mislocalization of ALK activity to MTs might influence downstream signalling and malignant properties of cells. Furthermore, the structure of EML4 TD may enable the development of protein-protein interaction inhibitors targeting the trimerization interface, providing a possible avenue towards therapeutic intervention in EML4-ALK NSCLC.
DOI Link: 10.1042/BJ20150039
ISSN: 0264-6021
eISSN: 1470-8728
Links: http://www.biochemj.org/bj/imps/abs/BJ20150039.htm
http://hdl.handle.net/2381/31855
Version: Post-print
Status: Peer-reviewed
Type: Journal Article
Rights: Archived with reference to SHERPA/RoMEO and publisher website. The final version of record is available at http://www.biochemj.org/bj/imps/abs/BJ20150039.htm
Description: We thank the beamline support staff at DLS I02 and I04 for assistance with data collection and the Centre for Core Biotechnology Services (University of Leicester) for imaging support.
Appears in Collections:Published Articles, Dept. of Biochemistry

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