The industrial workhorse fungus， ， is typically exploited for its ability to produce cellulase enzymes， whereas use of this fungus for over-expression of other proteins (homologous and heterologous) is still very limited. Identifying transformants expressing target protein is a tedious task due to low transformation efficiency， combined with highly variable expression levels between transformants. Routine methods for identification include PCR-based analysis， western blotting， or crude activity screening， all of which are time-consuming techniques. To simplify this screening， we have adapted the 2A peptide system from the foot-and-mouth disease virus (FMDV) to to express a readily screenable marker protein that is co-translated with a target protein. The 2A peptide sequence allows multiple independent genes to be transcribed as a single mRNA. Upon translation， the 2A peptide sequence causes a "ribosomal skip" generating two (or more) independent gene products. When the 2A peptide is translated， the "skip" occurs between its two -terminal amino acids (glycine and proline)， resulting in the addition of extra amino acids on the terminus of the upstream protein and a single proline addition to the terminus of the downstream protein. To test this approach， we have cloned two heterologous proteins on either side of a modified 2A peptide， a secreted cellobiohydrolase enzyme (Cel7A from ) as our target protein， and an intracellular enhanced green fluorescent protein (eGFP) as our marker protein. Using straightforward monitoring of eGFP expression， we have shown that we can efficiently monitor the expression of the target Cel7A protein.