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Ruiz, A.

Publications and source records attributed to Ruiz, A..

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Genome Wide Meta-Analysis identifies new loci associated with cardiac phenotypes and uncovers a common genetic signature shared by heart function and Alzheimer’s disease

AimsEchocardiography has become an indispensable tool for the study of heart performance, improving the monitoring of individuals with cardiac diseases. Diverse genetic factors associated with echocardiographic measures of heart structure and functions have been previously reported. The impact of several apoptotic genes in heart development identified in experimental models prompted us to assess their potential association with indicators of human cardiac function. This study started with the aim to investigate the possible association of variants of apoptotic genes with echocardiographic traits and to identify new genetic markers associated with cardiac function.\n\nMethods and resultsGenome wide data from different studies were obtained from public repositories. After quality control and imputation, association analyses confirm the role of caspases and other apoptosis related genes with cardiac phenotypes. Moreover, enrichment analysis showed an over-representation of genes, including some apoptotic regulators, associated with Alzheimers disease (AD). We further explored this unexpected observation which was confirmed by genetic correlation analyses.\n\nConclusionsOur findings show the association of apoptotic gene variants with echocardiographic indicators of heart function and reveal a novel potential genetic link between echocardiographic measures in healthy populations and cognitive decline later on in life. These findings may have important implications for preventative strategies combating Alzheimers disease.

genetics

Concomitant Duplication Of The Cid And Cenp-C Genes In Drosophila

The constitutive centromeric proteins CenH3 and Cenp-C are interdependent in their role of establishing centromere identity and function. In a recent paper, Kursel and Malik (February 2017; doi: 10.1093/molbev/msx091) reported that the Drosophila CenH3 homologue Cid underwent four independent duplication events during evolution. Particularly interesting is the duplication that took place in the common ancestor of the Drosophila subgenus and led to the subfunctionalization and high divergence of the Cid1 and Cid5 paralogs. Here, we describe another independent Cid duplication (Cid1 leading to Cid6) in the buzzatii cluster (repleta group) of the Drosophila subgenus. Moreover, we found that, in addition to the Cid1/Cid5 duplication, Cenp-C was also duplicated (Cenp-C1, Cenp-C2) in the common ancestor of the Drosophila subgenus. Analyses of expression and tests for positive selection indicate that both Cid5 and Cenp-C2 are male germline-biased and evolved adaptively, indicating subfunctionalization of the Cid and Cenp-C paralogs. Our findings further highlight the strong interdependence between CenH3 and Cenp-C, paving the way to new perspectives by which centromere function and evolution can be addressed.

genetics