Plant parasitism has evolved 12 times within flowering plants (Nickrent, 2020). This phylogenetic diversity is accompanied by a wide variety of habits, geographical distribution, host preferences, morphologies, and developmental patterns (Kuijt, 1969;Heide-Jørgensen, 2008). A broad spectrum of photosynthetic capabilities is also represented among these plants, ranging from species fully capable of photosynthesis, to those that are achlorophyllous during all or most of their life cycle, thus rendering them entirely reliant on host resources (Bromham et al., 2013). A subset of plants in the latter category exhibits a particularly extreme degree of reduction: their vegetative body is reduced to mycelium-like filaments of parenchyma cells embedded within their host tissues. In these cases, the parasite only becomes visible during reproduction when the flower/inflorescence temporarily emerges from its host (Mauseth, 1990;Meijer and Veldkamp, 1993;Nikolov et al., 2014b). Due to this extremely reduced growth form, restricted to life inside its host, these plants are commonly referred to as endoparasites.This highly modified and cryptic growth habit has been best described in detail from a small number of mistletoe species (Těšitel, 2016). Mistletoes are widely distributed parasitic plants known as keystone species in both natural and human-altered ecosystems (