19 research outputs found

    The origins and spread of domestic horses from the Western Eurasian steppes

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    This is the final version. Available on open access from Nature Research via the DOI in this recordData availability: All collapsed and paired-end sequence data for samples sequenced in this study are available in compressed fastq format through the European Nucleotide Archive under accession number PRJEB44430, together with rescaled and trimmed bam sequence alignments against both the nuclear and mitochondrial horse reference genomes. Previously published ancient data used in this study are available under accession numbers PRJEB7537, PRJEB10098, PRJEB10854, PRJEB22390 and PRJEB31613, and detailed in Supplementary Table 1. The genomes of ten modern horses, publicly available, were also accessed as indicated in their corresponding original publications57,61,85-87.NOTE: see the published version available via the DOI in this record for the full list of authorsDomestication of horses fundamentally transformed long-range mobility and warfare. However, modern domesticated breeds do not descend from the earliest domestic horse lineage associated with archaeological evidence of bridling, milking and corralling at Botai, Central Asia around 3500 BC. Other longstanding candidate regions for horse domestication, such as Iberia and Anatolia, have also recently been challenged. Thus, the genetic, geographic and temporal origins of modern domestic horses have remained unknown. Here we pinpoint the Western Eurasian steppes, especially the lower Volga-Don region, as the homeland of modern domestic horses. Furthermore, we map the population changes accompanying domestication from 273 ancient horse genomes. This reveals that modern domestic horses ultimately replaced almost all other local populations as they expanded rapidly across Eurasia from about 2000 BC, synchronously with equestrian material culture, including Sintashta spoke-wheeled chariots. We find that equestrianism involved strong selection for critical locomotor and behavioural adaptations at the GSDMC and ZFPM1 genes. Our results reject the commonly held association between horseback riding and the massive expansion of Yamnaya steppe pastoralists into Europe around 3000 BC driving the spread of Indo-European languages. This contrasts with the scenario in Asia where Indo-Iranian languages, chariots and horses spread together, following the early second millennium BC Sintashta culture

    Phytochelatins: Sulfur-Containing Metal(loid)-Chelating Ligands in Plants

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    Phytochelatins (PCs) are small cysteine-rich peptides capable of binding metal(loid)s via SH-groups. Although the biosynthesis of PCs can be induced in vivo by various metal(loid)s, PCs are mainly involved in the detoxification of cadmium and arsenic (III), as well as mercury, zinc, lead, and copper ions, which have high affinities for S-containing ligands. The present review provides a comprehensive account of the recent data on PC biosynthesis, structure, and role in metal(loid) transport and sequestration in the vacuoles of plant cells. A comparative analysis of PC accumulation in hyperaccumulator plants, which accumulate metal(loid)s in their shoots, and in the excluders, which accumulate metal(loid)s in their roots, investigates the question of whether the endogenous PC concentration determines a plant’s tolerance to metal(loid)s. Summarizing the available data, it can be concluded that PCs are not involved in metal(loid) hyperaccumulation machinery, though they play a key role in metal(loid) homeostasis. Unraveling the physiological role of metal(loid)-binding ligands is a fundamental problem of modern molecular biology, plant physiology, ionomics, and toxicology, and is important for the development of technologies used in phytoremediation, biofortification, and phytomining

    Translocation of Ni and Zn in Odontarrhena corsica and Noccaea caerulescens:the effects of exogenous histidine and Ni/Zn interactions

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    Aims: Nickel (Ni) and zinc (Zn) interactions during their uptake and root-to-shoot translocation and the potential role of histidine therein were studied in different populations of the Ni/Zn hyperaccumulator Noccaea caerulescens and the Ni hyperaccumulator Odontarrhena corsica. Methods: The effect of exogenous L-histidine supply on Ni and Zn uptake and translocation in N. caerulescens and O. corsica, and xylem loading in shoot-excised root systems of different N. caerulescens populations, were studied under separate and combined exposure. Results: In O. corsica, Zn inhibited both the translocation and the uptake of Ni, whereas Ni did not significantly affect Zn uptake or translocation. In N. caerulescens, both in intact plants and shoot-excised root systems, Zn usually inhibited the uptake, but not the translocation of Ni, whereas Ni did not affect the uptake, but inhibited the translocation of Zn, though not in two populations with low Zn xylem loading capacity. Exogenous histidine supply did not significantly affect Zn translocation in O. corsica and intact plants of an ultramafic population of N. caerulescens, but enhanced Zn xylem loading in two calamine populations of N. caerulescens and Ni translocation in all of them. Conclusions: High free L-histidine concentrations in roots might promote Ni hyperaccumulation in obligate Ni hyperaccumulators, such as O. corsica, in nature. The high histidine concentration in roots of N. caerulescens, which is primarily a Zn hyperaccumulator, might not only explain its species-wide conserved capacity to hypertranslocate Ni, but may also contribute to its Zn translocation capacity, at least in non-ultramafic populations

    Intra-specific variation in zinc, cadmium and nickel hypertolerance and hyperaccumulation capacities in Noccaea caerulescens

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    Aims: The study aimed at characterizing the patterns of natural variation in the tolerance and accumulation capacities for zinc (Zn), cadmium (Cd), and nickel (Ni) between and within edaphic ecotypes of the Zn/Cd/Ni hyperaccumulator, Noccaea caerulescens. Methods: Tolerance was assessed in a hydroponic ‘sequential exposure’ test, using the lowest concentration that completely arrested root growth as an end point. Accumulation was measured as the foliar metal concentration after six weeks of growth at 5 µM Zn, 2 µM Cd, or 1 µM Ni. Results: Zn and Cd tolerance were positively correlated, and highest in the calamine ecotype. Ni tolerance was without significant ecotypic variation. The ultramafic ecotype was as Zn-tolerant as the non-metallicolous one, but much more sensitive to Cd. The accumulation capacities for Zn, Cd and Ni were all positively correlated and without significant ecotypic variation. Zn hyperaccumulation capacity was species-wide, but Cd and Ni hyperaccumulation capacities were lacking in four populations (all calamine). Conclusions: There is considerable independent variation among populations regarding their Zn, Cd, and Ni accumulation capacities. This variation is most pronounced within the calamine ecotype, because some populations apparently had adopted an exclusion strategy for Zn or Cd hypertolerance, whereas others had not

    Zinc- and nickel-induced changes in fatty acid profiles in the zinc hyperaccumulator Arabidopsis halleri and non-accumulator Arabidopsis lyrata

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    This pilot study aimed at comparing zinc (Zn) and nickel (Ni) effects on the fatty acid (FA) profiles, oxidative stress and desaturase activity in the Zn hyperaccumulator Arabidopsis halleri and the excluder Arabidopsis lyrata to allow a better picture of the physiological mechanisms which may contribute to metal tolerance or acclimation. The most significant changes in the FA composition were observed in the shoots of the hyperaccumulator and in the roots of the excluder, and were not only metal-dependent, but also species-specific, since the most significant changes in the shoots of A. halleri were observed under Ni treatment, though Ni, in contrast to Zn, was accumulated mainly in its roots. Several FAs appeared in the roots and shoots of A. lyrata only upon metal exposure, whereas they were already found in control A. halleri. In both species, there was an increase in oleic acid under Ni treatment in both organs, whereas in Zn-treated plants the increase was shown only for the shoots. A rare conjugated α-parinaric acid was identified only in the shoots of metal-treated A. halleri. In the shoots of the hyperaccumulator, there was an increase in the content of saturated FAs and a decrease in the content of unsaturated FAs, while in the roots of the excluder, the opposite pattern was observed. These metal-induced changes in FA composition in the shoots of A. halleri can lead to a decrease in the fluidity of membranes, which could diminish the penetration of ROS into the membrane and thus maintain its stability

    Transcriptional effects of cadmium on iron homeostasis differ in calamine accessions of Noccaea caerulescens

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    Calamine accessions of the zinc/cadmium/nickel hyperaccumulator, Noccaea caerulescens, exhibit striking variation in foliar cadmium accumulation in nature. The Ganges accession (GA) from Southern France displays foliar cadmium hyperaccumulation (>1000 μg g−1 DW), whereas the accession La Calamine (LC) from Belgium, with similar local soil metal composition, does not (−1 DW). All calamine accessions are cadmium hypertolerant. To find out the differences between LC and GA in their basic adaptation mechanisms, we bypassed the cadmium excluding phenotype of LC by exposing the plants to 50 μm cadmium in hydroponics, achieving equal cadmium accumulation in the shoots. The iron content increased in the roots of both accessions. GA exhibited significant decreases in manganese and zinc contents in the roots and shoots, approaching those in LC. Altogether 702 genes responded differently to cadmium exposure between the accessions, 157 and 545 in the roots and shoots, respectively. Cadmium-exposed LC showed a stress response and had decreased levels of a wide range of photosynthesis-related transcripts. GA showed less changes, mainly exhibiting an iron deficiency-like response. This included increased expression of genes encoding five iron deficiency-regulated bHLH transcription factors, ferric reduction oxidase FRO2, iron transporters IRT1 and OPT3, and nicotianamine synthase NAS1, and decreased expression of genes encoding ferritins and NEET (a NEET family iron-sulfur protein), which is possibly involved in iron transfer, distribution and/or management. The function of the IRT1 gene in the accessions was compared. We conclude that the major difference between the two accessions is in the way they cope with iron under cadmium exposure.</p
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