Unveiling a Microexon Switch: Novel Regulation of the Activities of Sugar Assimilation and Plant-Cell-Wall-Degrading Xylanases and Cellulases by Xlr2 in Trichoderma virens .
Cynthia Coccet Castañeda-CasasolaMaría Fernanda Nieto-JacoboAmanda SoaresEmir Alejandro Padilla-PadillaMiguel Angel Anducho-ReyesWarren P TateSereyboth SothEdgardo Ulises Esquivel-NaranjoJohn G HamptonArtemio Mendoza-MendozaPublished in: International journal of molecular sciences (2024)
Functional microexons have not previously been described in filamentous fungi. Here, we describe a novel mechanism of transcriptional regulation in Trichoderma requiring the inclusion of a microexon from the Xlr2 gene. In low-glucose environments, a long mRNA including the microexon encodes a protein with a GAL4-like DNA-binding domain (Xlr2-α), whereas in high-glucose environments, a short mRNA that is produced encodes a protein lacking this DNA-binding domain (Xlr2-β). Interestingly, the protein isoforms differ in their impact on cellulase and xylanase activity. Deleting the Xlr2 gene reduced both xylanase and cellulase activity and growth on different carbon sources, such as carboxymethylcellulose, xylan, glucose, and arabinose. The overexpression of either Xlr2-α or Xlr2-β in T. virens showed that the short isoform (Xlr2-β) caused higher xylanase activity than the wild types or the long isoform (Xlr2-α). Conversely, cellulase activity did not increase when overexpressing Xlr2-β but was increased with the overexpression of Xlr2-α . This is the first report of a novel transcriptional regulation mechanism of plant-cell-wall-degrading enzyme activity in T. virens. This involves the differential expression of a microexon from a gene encoding a transcriptional regulator.
Keyphrases
- cell wall
- dna binding
- transcription factor
- copy number
- genome wide
- genome wide identification
- protein protein
- endothelial cells
- blood glucose
- gene expression
- type diabetes
- amino acid
- adipose tissue
- oxidative stress
- skeletal muscle
- drinking water
- dna methylation
- glycemic control
- weight loss
- heat shock
- genome wide analysis