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Claims of SS must demonstrate species sympatry, sister relationship, reproductive isolation, and that an earlier allopatric phase is highly unlikely (2).

We recently described two studies of SS in two evolutionarily divergent mammals, the blind subterranean mole rat , at “Evolution Canyon” (EC), Mount Carmel, Israel (5).

Gene ontology (GO) enrichment analysis revealed functions of musculature, energetics, metabolism, and sensory biology (Fig. In contrast, functions related to neurogenetics and nutrition were enriched in the chalk population (Fig. Our genome-wide scans for positive selection highlight how, where, and why adaptive evolution has shaped genetic variations.

Besides genomics, proteomics, particularly mechanisms regulating proteostasis, selectively drive soil population divergence.

The two abutting soil populations of in northern Israel habituate the ancestral Senonian chalk population and abutting derivative Plio-Pleistocene basalt population.

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A total of 14,539,199 SNPs were identified, with 3,717,338 and 3,361,317 SNPs unique to the basalt and chalk populations, respectively (Fig. We validated our SNP calling strategy with traditional Sanger sequencing technology and found that the genome-wide false-positive rate is less than 6% and the false-negative rate is less than 13% () based on all SNPs.

There are four species of was studied for whole genome analysis from the Alma Plio-Pleistocene basalt plateau vs. A total of 11 animals, 5 from chalk and 6 from basalt, were captured alive near Rehaniya, Upper Galilee (33.04E, 35.49N), in January 2014 (Fig.

1 using the DNeasy Blood and Tissue Kit (Qiagen) following the manufacturer’s protocol.

Importantly, distinctions in protein degradation may also contribute to SS.

Natural selection and natural genetic engineering [Shapiro JA (2011) ] overrule gene flow, evolving divergent ecological adaptive complexes.




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