Tip60 might be a candidate for the acetylation of hepatic carbonic anhydrase I and III in mice

Mol Biol Rep. 2021 Nov;48(11):7397-7404. doi: 10.1007/s11033-021-06753-8. Epub 2021 Oct 15.

Abstract

Background: Carbonic anhydrases (CAs) play a significant role in maintaining pH balance by catalyzing the conversion of carbon dioxide to bicarbonate. The regulation of pH is critical for all living organisms. Although there are many studies in the literature on the biochemical, functional, and structural features of CAs, there is not sufficient information about the epigenetic regulation of CAs.

Methods and results: The lysine acetyltransferase TIP60 (60 kDa Tat-interactive protein) was knocked out specifically in mouse liver using the Cre/loxP system, and knockout rate was shown as 83-88% by Southern blot analysis. The impact of Tip60 on the expression of Ca1, Ca3, and Ca7 was investigated at six Zeitgeber time (ZT) points in the control and liver-specific Tip60 knockout mice (mutant) groups by real-time PCR. In the control group, while Ca1 showed the highest expression at ZT8 and ZT12, the lowest expression profile was observed at ZT0 and ZT20. Hepatic Ca1 displayed robust circadian expression. However, hepatic Ca3 exhibited almost the same level of expression at all ZT points. The highest expression of Ca7 was observed at ZT12, and the lowest expression was determined at ZT4. Furthermore, hepatic Ca7 also showed robust circadian expression. The expression of Ca1 and Ca3 significantly decreased in mutant mice at all time periods, but the expression of Ca7 used as a negative control was not affected.

Conclusions: It was suggested for the first time that Tip60 might be considered a candidate protein in the regulation of the Ca1 and Ca3 genes, possibly by acetylation.

Keywords: Acetylation; Carbonic anhydrases; Circadian rhythm; Mice; Tip60.

MeSH terms

  • Acetylation
  • Animals
  • Carbonic Anhydrase I / metabolism*
  • Carbonic Anhydrase III / metabolism*
  • Circadian Rhythm*
  • Liver / metabolism*
  • Lysine Acetyltransferase 5 / genetics
  • Lysine Acetyltransferase 5 / metabolism*
  • Male
  • Mice
  • Mice, Knockout
  • Protein Processing, Post-Translational
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*

Substances

  • Trans-Activators
  • Kat5 protein, mouse
  • Lysine Acetyltransferase 5
  • Carbonic Anhydrase I
  • Carbonic Anhydrase III