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Skorecki, K.

Publications and source records attributed to Skorecki, K..

2 recordsLinked to original sources

Revisiting the lineages of the Cohanim using data from next-generation sequencing

BackgroundEarly studies using a handful of Y-chromosome markers showed that many self-declared Jewish priests (Cohanim) share related haplotypes, but the limited resolution left open how many priestly lineages exist, when they arose, and how they map onto Jewish population history. ObjectivesWe used whole-Y sequencing and modern phylogenetic tools to (i) catalogue Y-chromosome clades that are robustly enriched among Cohanim, (ii) date their most-recent common ancestors (TMRCAs) with pedigree-calibrated clocks, (iii) reconstruct their geographic dispersal across the Jewish Diaspora, and (iv) offer a stable, SNP-block nomenclature for future work. MethodsWe generated 104 new Big Y-700 sequences from rigorously documented Cohanim spanning 20 diaspora origins, and incorporated 215 legacy samples re-typed for diagnostic SNPs. Phylogenies and branch TMRCAs were built on the FTDNA and YFull backbones. A branch qualified as "Cohen" (CB) if [≥]5 men and [≥]50 % of branch members self-identified as Cohanim. ResultsNine Cohen branches met these criteria, and for the current study were designated CB-01 to CB-09 with numbering based on antiquity of SNP-block coalescence. CB-01 is the largest ([~]45 % of all Cohanim sampled), the most ancient (TMRCA {approx} 850 BCE), and the only lineage present in every major Jewish community. Its internal topology shows explosive branching between 700 and 300 BCE, stasis through the Roman-Byzantine era, and renewed expansion after 800 CE, mirroring known demographic pulses. CB-02 (TMRCA {approx} 700 BCE) and CB-03 ({approx} 550 BCE) likewise trace to Iron- or late Classical-period Judea but are geographically narrower. CB-04 - CB-07 are Near-Eastern clades whose priestly status may have crystallized 0-1000 CE, while CB-05, CB-08 and CB-09 appear to derive from Mediterranean host populations. Twenty percent of Cohanim fall outside any current CB, indicating that additional, rarer lineages remain to be characterized. ConclusionsHigh-resolution sequencing reveals a small set of divergent paternal lines comprising the Jewish priesthood, dominated by a pre-exilic Levantine lineage whose branch structure traces three millennia of geographically dispersed Jewish demographic history. The CB nomenclature, SNP catalogues and open dataset provided here supply a reproducible framework for genetic and historical studies which illustrate the broader power of dense uniparental phylogenies in population-genetic inference.

genomics↗

Apolipoprotein L1 Dynamics in Human Parietal Epithelial Cell Molecular Phenotype Kinetics

Human Parietal Epithelial cells (PECs) are considered as a source of progenitor cells to sustain podocyte (PD) homeostasis. We hypothesized that the absence of apolipoprotein (APO) L1 favors the PEC phenotype and that induction of APOL1 transitions to PD renewal. During PECs transition, APOL1 expression coincided with the expression of PD markers (PEC transition) along with down regulation of miR193a. The induction of APOL1 down regulated miR193a and induced PD markers in PECs/HEKs; whereas, the APOL1-silencing in transited (Tr)-PECs/HepG2s up regulated miR193a expression suggesting a reciprocally linked feedback loop relationship between APOL1 and miR193a. HIV, IFN-y, and vitamin D receptor agonist (VDA) induced APOL1 expression and PEC transition markers but down regulated miR193a in PECs/HEKs. Glomeruli in HIV patients and HIV: APOL1 transgenic mice displayed foci of PECs expressing synaptopodin, a PEC transition marker. Since APOL1 silencing in PECs partially attenuated HIV-, VDA-, and IFN-y-induced PECs transition, this would suggest that APOL1 is an important functional constituent of APOL1-miR193a axis.

molecular biology↗