Journal article

ATM substrate Chk2-interacting Zn 2 finger (ASCIZ) is a bi-functional transcriptional activator and feedback sensor in the regulation of dynein light chain (DYNLL1) expression

S Jurado, LA Conlan, EK Baker, JL Ng, N Tenis, NC Hoch, K Gleeson, M Smeets, D Izon, J Heierhorst

Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2012

Abstract

The highly conserved DYNLL1 (LC8) protein was originally discovered as a light chain of the dynein motor complex, but is increasingly emerging as a sequence-specific regulator of protein dimerization with hundreds of targets and wide-ranging cellular functions. Despite its important roles, DYNLL1's own regulation remains poorly understood. Here we identify ASCIZ (ATMIN/ZNF822), an essential Zn 2+ finger protein with dual roles in the DNA base damage response and as a developmental transcription factor, as a conserved regulator of Dynll1 gene expression. DYNLL1 levels are reduced by ∼10-fold in the absence of ASCIZ in human, mouse and chicken cells. ASCIZ binds directly to the Dynll1 promoter..

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Grants

Funding Acknowledgements

This work was supported by grants and a Senior Research Fellowship from the National Health and Medical Research Council (NHMRC) of Australia (to J. H.), a PhD scholarship from the Cooperative Research Centre Cancer Therapeutics (to S. J.), and in part by the Victorian Government's Operational Infrastructure Support Program.