Similarly, we found that in HeV-infected cells, HeV M localises to sub-nucleolar compartments (FC-DFC) early during infection (7 h post-infection (p.i.)), but becomes more diffuse in the nucleolus (i.e. accumulated into the GC), and with greater nuclear accumulation by 24 h p.i. (Figure 3a), consistent with observations for GFP HeV M WT protein and observations of dynamic nuclear/nucleolar localisation of M protein in NiV-infected cells [11]. This evidence concerns the gene MYOM2 and infection.