2017
DOI: 10.1007/s13127-016-0320-4
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Using multi-locus sequence data for addressing species boundaries in commonly accepted lichen-forming fungal species

Abstract: Using multi-locus sequence data for addressing species boundaries in commonly accepted lichen-forming fungal species.

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Cited by 25 publications
(19 citation statements)
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“…RNA‐sequencing analysis revealed numerous differentially expressed genes in Thellungiella salsuginea under cold treatment . RNA interference lines of the cold‐induced gene TsFtsH8 enhanced Thellungiella salsuginea tolerance to cold . Similarly, the Thellungiella salsuginea salt‐induced gene TsnsLTP4 encodes a non‐specific lipid transfer protein that participates in wax deposition and in plant tolerance against abiotic stresses, including salt, ABA, and high and low temperatures …”
Section: Temperature Changesmentioning
confidence: 99%
See 1 more Smart Citation
“…RNA‐sequencing analysis revealed numerous differentially expressed genes in Thellungiella salsuginea under cold treatment . RNA interference lines of the cold‐induced gene TsFtsH8 enhanced Thellungiella salsuginea tolerance to cold . Similarly, the Thellungiella salsuginea salt‐induced gene TsnsLTP4 encodes a non‐specific lipid transfer protein that participates in wax deposition and in plant tolerance against abiotic stresses, including salt, ABA, and high and low temperatures …”
Section: Temperature Changesmentioning
confidence: 99%
“…152,153 RNA interference lines of the cold-induced gene TsFtsH8 enhanced Thellungiella salsuginea tolerance to cold. 28,[154][155][156] Similarly, the Thellungiella salsuginea salt-induced gene TsnsLTP4 encodes a non-specific lipid transfer protein that participates in wax deposition and in plant tolerance against abiotic stresses, including salt, ABA, and high and low temperatures. [157][158][159][160] Distinct pathways mediate stress adaptation…”
Section: Salt Stressmentioning
confidence: 99%
“…Difficulties during sequencing of the mycobiont and lichenicolous fungi have been reported because universal DNA barcodes do not exist (Schoch et al, ). After testing several recent primer pairs and PCR conditions (Matheny, Liu, Ammirati, & Hall, ; Schmitt et al, ; Schoch et al, ; Westberg, Millanes, Knudsen, & Wedin, ; Williams et al, ; Zhao et al, ), the following final settings were used for the mycobiont: the primer pair ITS1f and LR3 (ITS) and gRPB1‐A and fRPB1‐C (RPB1) after Westberg et al () and Zhao et al () respectively. The lichenicolous fungi were inseparably connected to the lichen thallus and therefore always mixed with DNA of the mycobiont.…”
Section: Methodsmentioning
confidence: 99%
“…2,000 bases long mitochondrial ribosomal small subunit (mtSSU). This fragment, as delimited by the primers mtSSU1 and mtSSU3R (Zoller et al, 1999), is frequently used in lichen systematics and for species delimitation (Amo de Paz et al, 2011;Leavitt et al, 2015;Zhao et al, 2017;Kistenich et al, 2018). We designed a set of seven forward and seven reverse primers (Table 2; Figure 2) covering all of the 900 bases using Primer3 v. 2.3 (Untergasser et al, 2012) based on mtSSU sequences for our selected taxa or closely related taxa available from GenBank (Benson et al, 2018).…”
Section: Primer Design and Pcr Amplificationmentioning
confidence: 99%