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Gupta S , Kelow S , Wang L , Andrake M , Dunbrack RL Jr , Kruger WD
Mouse modeling and structural analysis of the p.G307S mutation in human cystathionine beta-synthase (CBS) reveal effects on CBS activity but not stability
J Biol Chem. 2018 Sep 7;293(36) :13921-13931
PMID: 30030379    PMCID: PMC6130948    URL: https://www.ncbi.nlm.nih.gov/pubmed/30030379
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Mutations in the cystathionine beta-synthase (CBS) gene are the cause of classical homocystinuria, the most common inborn error in sulfur metabolism. The p.G307S mutation is the most frequent cause of CBS deficiency in Ireland, which has the highest prevalence of CBS deficiency in Europe. Individuals homozygous for this mutation tend to be severely affected and are pyridoxine nonresponsive, but the molecular basis for the strong effects of this mutation is unclear. Here, we characterized a transgenic mouse model lacking endogenous Cbs and expressing human p.G307S CBS protein from a zinc-inducible metallothionein promoter (Tg-G307S Cbs(-/-)()) Unlike mice expressing other mutant CBS alleles, the Tg-G307S transgene could not efficiently rescue neonatal lethality of Cbs-/- in a C57BL/6J background. In a C3H/HeJ background, zinc-induced Tg-G307S Cbs(-/-) mice expressed high levels of p.G307S CBS in the liver, and this protein variant forms multimers similarly to mice expressing WT human CBS. However, the p.G307S enzyme had no detectable residual activity. Moreover, treating of mice with proteasome inhibitors failed to significantly increase in CBS-specific activity. These findings indicated that the G307S substitution likely affects catalytic function as opposed to causing a folding defect. Using molecular dynamics simulation techniques, we found that the G307S substitution likely impairs catalytic function by limiting the ability of the tyrosine at position 308 to assume the proper conformational state(s) required for the formation of the pyridoxal-cystathionine intermediate. These results indicate that the p.G307S CBS is stable but enzymatically inert and therefore unlikely to respond to chaperone-based therapy.
1083-351x Gupta, Sapna Kelow, Simon Wang, Liqun Andrake, Mark ORCID: https://orcid.org/0000-0003-2957-4350 Dunbrack, Roland L Jr Kruger, Warren D ORCID: https://orcid.org/0000-0002-4990-3695 Journal Article United States J Biol Chem. 2018 Jul 20. pii: RA118.002164. doi: 10.1074/jbc.RA118.002164.