consisting of diploids (for example,A. thaliana, Ath), autotetraploids (A. arenosa, Aar andA. lyrata, Aly) and allotetraploids such asA. suecica(Asu)15andA. kamchatica(Aka); the latter was formed betweenA. lyrataandA. halleri(Aha)16. Asu (AATT, 2n = 4x = 26) was forme...
This transporter is probably involved in zinc tolerance in the zinc hyperaccumulator Arabidopsis halleri (35). AtNramp3 and AtNramp4 have been shown recently to be present in the tonoplast and to participate specifically in iron mobilization from vacuolar metal stores during seed germination (36, ...
some of them not concurring with increased Zn tolerance, are likely to take place for the up to five paralogs of theMTP1inA. halleri30,48,49. Our study suggests that the relatedMTPA2has also played a role in the adaptive evolution of Zn ...
halleri are not strikingly different in hyperaccumulation and tolerance, but rather there is a continuous variation in natural populations (Pauwels et al., 2007). Therefore, segregation is better observed in interspecific crosses, usually performed with Arabidopsis lyrata ssp. petraea (L.) O’Kane ...
Recent and ancient signature of balancing selection around the S-locus in Arabidopsis halleri and A. lyrata. Mol Biol Evol 30: 435–447. Heredity Loss of self-incompatibility in Arabidopsis lyrata BK Mable et al Schierup MH, Bechsgaard JS, Christiansen FB (2008). Selection at work in self...
C. et al. Population genomic footprints of selection and associations with climate in natural populations of Arabidopsis halleri from the Alps. Molecular ecology 22, 5594–5607, doi: 10.1111/mec.12521 (2013). 4. Savolainen, O., Lascoux, M. & Merila, J. Ecological genomics of local ...