<mods:mods version="3.3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mods:titleInfo><mods:title>The role of GRAS-domain proteins in arbuscular mycorrhizal symbiosis</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">Leonie</mods:namePart><mods:namePart type="family">Luginbuehl</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>A major limitation to plant growth is the restricted access to nutrients in the soil. To&#13;
improve nutrient acquisition, the majority of land plants enter a beneficial symbiosis&#13;
with arbuscular mycorrhizal (AM) fungi. The accommodation of fungal hyphae in roots&#13;
requires the extensive transcriptional reprogramming of host cells. Several GRASdomain&#13;
proteins, including NSP1 (NODULATION SIGNALLING PATHWAY 1), NSP2, and&#13;
RAM1 (REQUIRED FOR ARBUSCULAR MYCORRHIZATION 1), have emerged as&#13;
important transcriptional regulators during mycorrhization. Interaction studies suggest&#13;
that these proteins form multicomponent complexes, raising the question whether they&#13;
regulate similar or different mycorrhizal processes. Here, the functions of NSP1, NSP2&#13;
and RAM1 during AM development were investigated by detailed phenotypic and&#13;
transcriptional analyses of the corresponding loss‐of‐function mutants.&#13;
Global gene expression profiling of nsp1‐1 revealed that NSP1 is required for the&#13;
expression of a large number of genes involved in strigolactone and gibberellin&#13;
biosynthesis at the pre‐contact stage of AM development. Strigolactones are known to&#13;
attract the fungus to the root. In line with this, the quantification of mycorrhizal&#13;
structures showed a delay in mycorrhization in nsp1‐1. Transcriptional profiling&#13;
confirmed that the expression of the majority of mycorrhizal‐induced genes was&#13;
delayed, but not abolished in nsp1‐1, suggesting that NSP1 only has a minor role in the&#13;
transcriptional regulation once the contact between the fungus and the roots has been&#13;
established. Unlike NSP1, RAM1 plays a critical role in the transcriptional regulation at&#13;
later stages of AM symbiosis. Mycorrhization was strongly impaired in ram1‐1, and&#13;
transcriptional profiling revealed that RAM1 is essential for the expression of several&#13;
genes involved in arbuscule development and the nutrient exchange between the&#13;
symbionts. Meanwhile, the exact function of NSP2 remains unclear, as no effect on&#13;
mycorrhization was observed in nsp2‐2 under the conditions tested here. These findings&#13;
suggest that NSP1, NSP2 and RAM1 play largely different roles in the transcriptional regulation during AM development.</mods:abstract><mods:originInfo><mods:dateIssued encoding="iso8601">2016-10</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>University of East Anglia;School of Biological Sciences</mods:publisher></mods:originInfo><mods:genre>Thesis</mods:genre></mods:mods>