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Post-translational modifications regulate signalling by Ror1

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KAUCKÁ Markéta KREJČÍ Pavel PLEVOVÁ Karla PAVLOVÁ Šárka PROCHÁZKOVÁ Jiřina JANOVSKÁ Pavlína VALNOHOVÁ Jana KOZUBÍK Alois POSPÍŠILOVÁ Šárka BRYJA Vítězslav

Druh Článek v odborném periodiku
Časopis / Zdroj Acta Physiologica
Fakulta / Pracoviště MU

Lékařská fakulta Přírodovědecká fakulta Středoevropský technologický institut

Citace
Doi http://dx.doi.org/10.1111/j.1748-1716.2011.02306.x
Obor Genetika a molekulární biologie
Klíčová slova Ror1; posttranslational modifications; glycosylation; chronic lymphocytic leukemia
Popis Ror1 (receptor tyrosine kinase-like orphan receptor)is highly upregulated in B cells of patients with chronic lymphocytic leukaemia (CLL). Ror1 acts as the Wnt receptor in the non-canonical Wnt pathway. We demonstrate that Ror1 is extensively modified by N-linked glycosylation. Glycosylation produces several variants of Ror1 with electrophoretic migration of approx. 100, 115 and 130 kDa. Inhibition of glycosylation interferes with cell surface localization of the 130-kDa variant of Ror1 and prevents Ror1-induced formation of filopodia. Moreover, we show that 130-kDa Ror1 is mono-ubiquitinated. Furthermore, individual CLL patients show striking differences in the electrophoretic migration of Ror1, which correspond to the level of glycosylation. Our data show that Ror1 undergoes complex post-translational modifications by glycosylation and mono-ubiquitination. These modifications regulate Ror1 localization and signalling, and are highly variable among individual CLL patients. These may suggest that Ror1 signals only in a subset of CLL patients despite Ror1 levels are ubiquitously high in all CLL patients.
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