Biochemical Characterisation of the Short Isoform of Histone N-Terminal Acetyltransferase NAA40

N-alpha-acetyltransferase 40 (NAA40) is an evolutionarily conserved N-terminal acetyltransferase (NAT) linked to oncogenesis and chemoresistance. A recent study reported the generation of a second, shorter NAA40 isoform (NAA40<sup>S</sup>) through alternative translation, which we proceeded to further characterise. Notably, recombinant NAA40<sup>S</sup> had a greater in vitro enzymatic activity and affinity towards its histone H2A/H4 substrates compared to full-length NAA40 (NAA40<sup>L</sup>). Within cells, NAA40<sup>S</sup> was enzymatically active, based on its ability to suppress the H2A/H4S1Ph antagonistic mark in CRISPR-generated <i>NAA40</i> knockout cells. Finally, we show that in addition to alternative translation, the NAA40<sup>S</sup> isoform could be derived from a primate and testis-specific transcript, which may align with the "out-of-testis" origin of recently evolved genes and isoforms. To summarise, our data reveal an even greater functional divergence between the two NAA40 isoforms than had been previously recognised.

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Publication Details

Journal
Biomolecules
Published
2024-09-02
DOI
https://doi.org/10.3390/biom14091100
Citations
4
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
1.13

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article

Biochemical Characterisation of the Short Isoform of Histone N-Terminal Acetyltransferase NAA40

Cem Özdemir, Costas Koufaris, Vicky Nicolaidou, Ariel Klavaris et al.
4 citations
Biomolecules
Peptidase Inhibition and Analysis
1.13
article

Biochemical Characterisation of the Short Isoform of Histone N-Terminal Acetyltransferase NAA40

Cem Özdemir, Costas Koufaris, Vicky Nicolaidou, Ariel Klavaris, Antonis Kirmizis, Kyle M. Miller, Maria Kouma
article en
4 citations

Abstract

N-alpha-acetyltransferase 40 (NAA40) is an evolutionarily conserved N-terminal acetyltransferase (NAT) linked to oncogenesis and chemoresistance. A recent study reported the generation of a second, shorter NAA40 isoform (NAA40<sup>S</sup>) through alternative translation, which we proceeded to further characterise. Notably, recombinant NAA40<sup>S</sup> had a greater in vitro enzymatic activity and affinity towards its histone H2A/H4 substrates compared to full-length NAA40 (NAA40<sup>L</sup>). Within cells, NAA40<sup>S</sup> was enzymatically active, based on its ability to suppress the H2A/H4S1Ph antagonistic mark in CRISPR-generated <i>NAA40</i> knockout cells. Finally, we show that in addition to alternative translation, the NAA40<sup>S</sup> isoform could be derived from a primate and testis-specific transcript, which may align with the "out-of-testis" origin of recently evolved genes and isoforms. To summarise, our data reveal an even greater functional divergence between the two NAA40 isoforms than had been previously recognised.

BiomoleculesVol. 14(9)
University of Nicosia (CY), University of Cyprus (CY), The University of Texas at Austin (US)
Cancer Research Institute, Cancer Prevention and Research Institute of Texas, University of Cyprus, Research and Innovation Foundation, European Regional Development Fund, National Cancer Institute
Openalex Percentile: Top 18%
Peptidase Inhibition and Analysis
1.13
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Biochemical Characterisation of the Short Isoform of Histone N-Terminal Acetyltransferase NAA40 — Cem Özdemir, Costas Koufaris, et al. · Biomolecules (2024) | TGRS Research Map | TGRS