Publications by authors named "Fabio Anaclerio"

Background: The complex interspersed pattern of segmental duplications in humans is responsible for rearrangements associated with neurodevelopmental disease, including the emergence of novel genes important in human brain evolution. We investigate the evolution of LCR16a, a putative driver of this phenomenon that encodes one of the most rapidly evolving human-ape gene families, nuclear pore interacting protein (NPIP).

Results: Comparative analysis shows that LCR16a has independently expanded in five primate lineages over the last 35 million years of primate evolution.

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Article Synopsis
  • The study focuses on a primate-specific gene family, known as POTEs, that is expressed in reproductive organs and several cancers like breast, prostate, and lung cancer, suggesting their potential roles as oncogenes, therapeutic targets, and biomarkers.
  • Researchers used advanced techniques, including single-molecule sequencing and comparative analysis, to investigate the structure, copy number, and distribution of POTE genes in primates, uncovering significant details about their evolution.
  • The findings include the first successful identification and assembly of a POTE gene duplication in marmosets, which was misrepresented in reference genomes, offering new insights into gene duplications and alterations in primate evolution.
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Grapevine (Vitis vinifera L.) is one of the world's most important crop plants, which is of large economic value for fruit and wine production. There is much interest in identifying genomic variations and their functional effects on inter-varietal, phenotypic differences.

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Gibbons are small arboreal apes that display an accelerated rate of evolutionary chromosomal rearrangement and occupy a key node in the primate phylogeny between Old World monkeys and great apes. Here we present the assembly and analysis of a northern white-cheeked gibbon (Nomascus leucogenys) genome. We describe the propensity for a gibbon-specific retrotransposon (LAVA) to insert into chromosome segregation genes and alter transcription by providing a premature termination site, suggesting a possible molecular mechanism for the genome plasticity of the gibbon lineage.

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