PubMed · 13488167
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G BUCCELLATO. [Lichen].. https://pubmed.ncbi.nlm.nih.gov/13488167/
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In the lichen symbiosis, the fungal and algal partners constitute a closely integrated system. The combination of fungal and algal partners changes along climate gradients in many species, and is expected to be adaptive. However, the functional mechanisms behind this symbiosis-mediated environmental adaptation are unknown. We investigated which transcriptional profiles are associated with specific fungal-algal symbiont pairings found in lichens from high-elevation (Lower Supratemperate) and low-elevation (Lower Mesomediterranean) sites at two extremes of a climatic gradient on Mount Limbara, Sardinia. Using laboratory-acclimatized thalli, we found that lichen fungal and algal symbionts show variable expression profiles between high- and low-elevation individuals: circadian- and temperature-associated genes for fungi and light-responsive genes for algae show climate-specific patterns. High- and low-elevation individuals differentially express sugar transporters in both symbionts, pointing to symmetrical and climate-dependent sugar transport mechanisms between them. A light pulse treatment identified asymmetries between fungal and algal light responses, with high- and low-elevation fungal symbionts but only low-elevation algal symbionts showing a response. Together, these results tie previously observed genomic variation along climatic gradients in a lichen species to functional differences in transcription for the fungal and algal symbionts, contributing to our understanding of environmental specialization and niche-specific partner combinations in lichens.
Spore-derived mycobionts of the lichen Graphis scripta var. serpentina and G. rikuzensis were cultivated on a malt-yeast extract medium supplemented with 10% sucrose and their metabolites were investigated. 3,3'-Dihydroxy-5,5'-dimethyldiphenyl ether was isolated from the cultures of the mycobionts of G. scripta var. serpentina, while a new phenyl ether, rikuzenol, along with two known diphenyl ethers, violaceol-I and violaceol-II, were isolated from those of G. rikuzensis. The structure of the new compound was determined by spectroscopic methods. Violaceol-I was chemically synthesized and interconversion between violaceol-I and violaceol-II was proven.
Two isofuranonaphthoquinone derivatives, named arthoniafurones A (1-acetyl-8-hydroxynaphtho[2,3-c]furan-4,9-dione) and B [1-acetyl-4,8-dihydroxynaphtho[2,3-c]furan-9(4H)-one], were isolated from a spore-derived culture of the mycobiont of the lichen Arthonia cinnabarina, that is new to Japan. Bostrycoidin and 8-O-methylbostrycoidin were also identified in the A. cinnabarina culture.