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- Rosser, Z H, et al.
(author)
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Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language.
- 2000
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In: American Journal of Human Genetics. - : Elsevier BV. - 0002-9297 .- 1537-6605. ; 67:6, s. 1526-43
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Journal article (peer-reviewed)abstract
- Clinal patterns of autosomal genetic diversity within Europe have been interpreted in previous studies in terms of a Neolithic demic diffusion model for the spread of agriculture; in contrast, studies using mtDNA have traced many founding lineages to the Paleolithic and have not shown strongly clinal variation. We have used 11 human Y-chromosomal biallelic polymorphisms, defining 10 haplogroups, to analyze a sample of 3,616 Y chromosomes belonging to 47 European and circum-European populations. Patterns of geographic differentiation are highly nonrandom, and, when they are assessed using spatial autocorrelation analysis, they show significant clines for five of six haplogroups analyzed. Clines for two haplogroups, representing 45% of the chromosomes, are continentwide and consistent with the demic diffusion hypothesis. Clines for three other haplogroups each have different foci and are more regionally restricted and are likely to reflect distinct population movements, including one from north of the Black Sea. Principal-components analysis suggests that populations are related primarily on the basis of geography, rather than on the basis of linguistic affinity. This is confirmed in Mantel tests, which show a strong and highly significant partial correlation between genetics and geography but a low, nonsignificant partial correlation between genetics and language. Genetic-barrier analysis also indicates the primacy of geography in the shaping of patterns of variation. These patterns retain a strong signal of expansion from the Near East but also suggest that the demographic history of Europe has been complex and influenced by other major population movements, as well as by linguistic and geographic heterogeneities and the effects of drift.
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| 2. |
- Rice, Ritva, et al.
(author)
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Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.
- 2004
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In: Journal of Clinical Investigation. - 0021-9738. ; 113:12, s. 1692-1700
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Journal article (peer-reviewed)abstract
- Classical research has suggested that early palate formation develops via epithelial-mesenchymal interactions, and in this study we reveal which signals control this process. Using Fgf10-/-, FGF receptor 2b-/- (Fgfr2b-/-), and Sonic hedgehog (Shh) mutant mice, which all exhibit cleft palate, we show that Shh is a downstream target of Fgf10/Fgfr2b signaling. Our results demonstrate that mesenchymal Fgf10 regulates the epithelial expression of Shh, which in turn signals back to the mesenchyme. This was confirmed by demonstrating that cell proliferation is decreased not only in the palatal epithelium but also in the mesenchyme of Fgfr2b-/- mice. These results reveal a new role for Fgf signaling in mammalian palate development. We show that coordinated epithelial-mesenchymal interactions are essential during the initial stages of palate development and require an Fgf-Shh signaling network.
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- Tedengren, Michael, et al.
(author)
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Heat pretreatment increase cadmium resistance and HSP 70 levels in Baltic Sea mussels
- 2000
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In: Aquatic Toxicology. - 0166-445X .- 1879-1514. ; 48:1, s. 1-12
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Journal article (peer-reviewed)abstract
- The effects of heat treatment and cadmium exposure on the synthesis of a major stress inducible protein (hsp 70) and on the metabolism of the blue mussel Mytilus edulis L. from the Baltic Sea, were studied in a laboratory experiment. The mussels were kept in sea water of ambient salinity (6.3‰) and temperature (4°C). The effects of cadmium (20 μg l−1), measured as changes in physiological rates (oxygen consumption, ammonia excretion, clearance rates and scope for growth) and hsp 70 expression were studied at 4°C and in combination with a rapid rise in temperature to 20°C. Relatively low levels of hsp 70 were detected but the negative effect was reflected in a reduction of scope for growth of the exposed mussels compared to controls. This effect was more pronounced at 20°C. Mussels not exposed to cadmium in the first experiment were used in a second set of experiments. Heat shocked mussels were allowed to reacclimatise to 4°C for 5 days and then, along with the mussels already at 4°C, exposed to cadmium (20 μg l−1). The results clearly indicated that the mussels exposed to 20°C in the first experiment more rapidly induced synthesis of hsp 70 after cadmium exposure in the second experiment. Also the reacclimatised mussels exposed to heat shock but not to cadmium in the first experiment, induced some hsp 70 in the second experiment. This suggests that the rate of induction of heat shock or stress proteins in Baltic mussels is slower than what has been described for mussels from more marine environments. The mussels kept at 4°C throughout the experiment and exposed to cadmium showed low levels of hsp 70, again indicating a low rate of induction. The increasing levels of hsp 70 correlated well with a maintained level of physiological fitness, in terms of scope for growth, although the mussels showed increasing body burdens of cadmium.
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