Penicillium oxalicum putative methyltransferase Mtr23B has similarities and differences with LaeA in regulating conidium development and glycoside hydrolase gene expression.

• LaeA-like methyltransferase Mtr23B contributes to spore pigment formation and the expression of secondary metabolic gene cluster and glycoside hydrolase genes in P. oxalicum. • Mtr23B has similarities and differences with LaeA in regulating the above biological processes. • LaeA interacts with VeA, while Mtr23B does not interact with VeA directly. Mtr23B may regulate cellulase and amylase gene transcription by interacting with HAP5 and chromatin remodeling complex. Putative methyltranferase LaeA and LaeA-like proteins, which are conserved in many filamentous fungi, regulate the sporogenesis and biosynthesis of secondary metabolites. In this study, we reported the biological function of a LaeA-like methyltransferase, Penicillium oxalicum Mtr23B, which contains a methyltransf_23 domain and an S-adenosylmethionine binding domain, in controlling spore pigment formation and in the expression of secondary metabolic gene cluster and glycoside hydrolase genes. Additionally, we compared Mtr23B and LaeA, and determined their similarities and differences in terms of their roles in regulating the above biological processes. mtr23B had the highest transcriptional level among the 12 members of the methyltransf_23 family in P. oxalicum. The colony color of Δ mtr23B (deletion of mtr23B) was lighter than that of Δ laeA , although Δ mtr23B produced ~ 19.2-fold more conidia than Δ laeA. The transcriptional levels of abrA , abrB / yA , albA / wA , arpA , arpB , and aygA , which are involved in the dihydroxynaphtalene–melanin pathway, decreased in Δ mtr23B. However, Mtr23B had a little effect on brush-like structures and conidium formation, and had a different function from LaeA. Mtr23B extensively regulated glycoside hydrolase gene expression. The absence of Mtr23B remarkably repressed prominent cellulase- and amylase-encoding genes in the whole culture period, while the effect of LaeA mainly occurred in the later phases of prolonged batch cultures. Similar to LaeA, Mtr23B was involved in the expression of 10 physically linked regions containing secondary metabolic gene clusters; the highest regulatory activities of Mtr23B and LaeA were observed in BrlA-dependent cascades. Although LaeA interacted with VeA, Mtr23B did not interact with VeA directly. We assumed that Mtr23B regulates cellulase and amylase gene transcription by interacting with the CCAAT-binding transcription factor HAP5 and chromatin remodeling complex. [ABSTRACT FROM AUTHOR]