Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

Abstract

Purpose: CAG/CAA repeat expansions in TBP_>49 are responsible for spinocerebellar ataxia (SCA) type 17 (SCA17). We previously detected cosegregation of STUB1 variants causing SCA48 with intermediate alleles of TBP in 2 families. This cosegregation questions the existence of SCA48 as a monogenic disease.

Methods: We systematically sequenced TBP repeats in 34 probands of dominant ataxia families with STUB1 variants. In addition, we searched for pathogenic STUB1 variants in probands with expanded alleles of TBP_>49 (n = 2) or intermediate alleles of TBP_≥40 (n = 47).

Results: STUB1 variants were found in half of the TBP_40-49 cohort. Mirroring this finding, TBP_40-49 alleles were detected in 40% of STUB1 probands. The longer the TBP repeat length, the more likely the occurrence of cognitive impairment (P = .0129) and the faster the disease progression until death (P = .0003). Importantly, 13 STUB1 probands presenting with the full SCA48 clinical phenotype had normal TBP_37-39 alleles, excluding digenic inheritance as the sole mode.

Conclusion: We show that intermediate TBP_40-49 alleles act as disease modifiers of SCA48 rather than a STUB1/TBP digenic model. This distinction from what has been proposed before has crucial consequences for genetic counseling in SCA48.

Keywords: SCA17; SCA48; STUB1, Spinocerebellar ataxia; TBP.