Multiple TSC22D4 iso‐/phospho‐glycoforms display idiosyncratic subcellular localizations and interacting protein partners

• Published in: The FEBS journal 2013-03, Vol.280 (5), p.1320-1329
• Main Authors: Canterini, Sonia, Carletti, Valentina, Nusca, Stefania, Mangia, Franco, Fiorenza, Maria Teresa
• Format: Article
• Language: English
• Subjects: Alternative Splicing; Animals; Animals, Newborn; Apoptosis Inducing Factor - metabolism; Biochemistry; Blotting, Western; Cell Nucleus - metabolism; Cellular biology; Cerebellum - cytology; Cerebellum - metabolism; chromatin; Chromatin - genetics; Cytoplasmic Granules - metabolism; Glycosylation; Immunoprecipitation; Mice; mitochondria; Mitochondria - metabolism; Neurons - cytology; Neurons - metabolism; nuclear matrix; Phosphorylation; Protein Isoforms; Protein Processing, Post-Translational; Proteins; Subcellular Fractions; Transcription Factors - genetics; Transcription Factors - metabolism; TSC22D4–TSC22D1/AIF heterodimers; TSC‐22 domain
• ISSN: 1742-464X; 1742-4658
• DOI: 10.1111/febs.12123

Proteins of the TSC22 domain (TSC22D) family, including TSC22D1 and TSC22D4, play pivotal roles in cell proliferation, differentiation and apoptosis, interacting with other factors in a still largely unknown manner. This study explores this issue by biochemically characterizing various TSC22D4 forms (both iso‐ and glyco‐phospho‐, namely the splice variants 42 and 55 kDa and the post‐translationally modified 67 and 72 kDa forms) and their subcellular localization and protein partners during cerebellar granule neuron (CGN) differentiation. The TSC22D4‐42 form is mostly cytosolic, and is the only TSC22D4 form that associates with TSC22D1.2 in undifferentiated but not differentiated CGNs. In contrast, TSC22D4‐55 is prominently associated with the nuclear matrix in differentiated but not undifferentiated CGNs. As for TSC22D4‐67, it is localized in the cytosol and nuclei of undifferentiated CGNs and enters mitochondria of differentiated CGNs, associating with apoptosis‐inducing factor. TSC22D4‐72 is modified by O‐linked beta‐N‐acetylglucosamine (O‐GlcNAcylated) and phosphorylated and is always associated with chromatin irrespective of CGN differentiation. The various subcellular localization patterns and interacting protein partners of TSC22D4 forms during CGN differentiation suggest the existence of form‐specific function(s) and provide a novel framework to further investigate the biological functions of TSC22D proteins. Structured digital AIF and TSC22D4 colocalize by cosedimentation (View interaction). TSC22D1 physically interacts with TSC22D4 by anti bait coimmunoprecipitation (View Interaction: 1, 2). TSC22D4 physically interacts with AIF by anti bait coimmunoprecipitation (View Interaction: 1, 2). AIF and TSC22D4 colocalize by cosedimentation (View interaction). Proteins of TSC22 domain family play isoform‐specific roles in cell proliferation, differentiation and apoptosis. We have characterized the nature, subcellular localizations and protein partners of TSC22D4 splice variants TSC22D4‐42 and TSC22D4‐55 and glyco‐phospho‐forms TSC22D4‐67 and TSC22D4‐72. TSC22D4‐42 and TSC22D4‐67 associate with TSC22D1.2 and mitochondrial AIF, respectively, depending on neuronal differentiation. TSC22D4‐72 and TSC22D4‐55 are stably chromatin‐ and nuclear matrix‐associated, respectively