Journal article

A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain

SL Williamson, L Giudici, C Kilstrup-Nielsen, W Gold, GJ Pelka, PPL Tam, A Grimm, D Prodi, N Landsberger, J Christodoulou

Human Genetics | SPRINGER | Published : 2012

Abstract

The X-linked cyclin-dependent kinase-like 5 (CDKL5) gene is an important molecular determinant of early-onset intractable seizures with infantile spasms and Rett syndrome-like phenotype. The gene encodes a kinase that may influence components of molecular pathways associated with MeCP2. In humans there are two previously reported splice variants that differ in the 5′ untranslated exons and produce the same 115 kDa protein. Furthermore, very recently, a novel transcript including a novel exon (16b) has been described. By aligning both the human and mouse CDKL5 proteins to the orthologs of other species, we identified a theoretical 107 kDa isoform with an alternative C-terminus that terminates..

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University of Melbourne Researchers

Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

We would like to express our gratitude to the Rett Syndrome Australian Research Fund, the Italian association proRETT ricerca, the Rotary Club of Narellan, the Harrington Park Foundation, and the Country Women's Association of NSW for additional financial support. This research was funded by National Health and Medical Research Council of Australia project grants 346603 (PT, JC) and 570752 (PT, JC), the E-Rare EuroRETT Network (NL), Fondazione Cariplo 2010-0724 (NL), the Italian Ministry of Research (CKN), and FP7-PEOPLE-ITN-2008 (CKN).