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Pellegrino, I.

Publications and source records attributed to Pellegrino, I..

2 recordsLinked to original sources

Profiling and Targeting of Regulatory RNAs to Upregulate Gene Expression

Transcription of long noncoding RNAs (lncRNAs), including enhancer RNAs (eRNAs) and promoter-associated RNAs (paRNAs), collectively termed regulatory RNAs (regRNAs), is a hallmark of active gene expression, yet it remains unknown whether regRNAs can be targeted to selectively enhance transcription in cis. We developed regRNA Capture-seq, a high-throughput method to profile regRNAs, and applied it to primary human hepatocytes, annotating thousands of regRNAs at [~]2,000 enhancers and promoters. Using this approach, we interrogated a genetically validated enhancer of the ornithine transcarbamylase (OTC) gene, mutations of which cause OTC deficiency (OTCD), the most common urea cycle disorder. Antisense oligonucleotides (ASOs) targeting enhancer-derived regRNAs led to dose-dependent upregulation of OTC in hepatocytes. Mechanistically, ASOs altered regRNA structure, elevated regRNA levels, displaced transcriptional repressors, and increased H3K27 acetylation at the targeted enhancer. This work establishes a potential therapeutic strategy for addressing haploinsufficiency and highlights regRNAs as actionable targets for ASO-mediated upregulation of gene expression.

genomics↗

Phylogeography of Lanius senator reveals conflicts between alpha taxonomy, subspecies ranges and genetics.

Implementing the effort in understanding biogeographic distribution patterns and taxonomic limits within animal groups is crucial for addressing several challenges of modern zoology. Although avian phylogeography has been deeply investigated within Western Palearctic, several families, such as shrikes, still display complicated or neglected biogeographic patterns both between and within species, thus requiring further investigations. The Woodchat Shrike (Lanius senator) is a long-distance migratory species that exhibits three morphologically well-recognizable subspecies, whose boundaries have never been molecularly investigated. Here, we aimed to define the phylogeographic structure of Lanius senator throughout its breeding range and assess the genetic coherence with the phenotypically described subspecies. We assembled a collection of 34 samples mainly from breeding populations of each subspecies and analyzed them at four mtDNA and two nuDNA markers. We did not find a clear phylogenetic structure with nuclear Ornithine Decarboxylase (ODC) and myoglobin intron 2 (MYO), while all the four mtDNA loci (i.e., ND2, COI, cytb and Control Region) highlighted two main haplogroups, one including both the nominate subspecies L. s. senator and L. s. badius and the second consistent with L. s. niloticus only from the easternmost part of the range. Surprisingly, individuals phenotypically assigned to L. s. niloticus from Israel were genetically assigned to the senator/badius haplogroup. Moreover, genetic distances showed intermediate values between inter-intraspecies diversity usually found in Passerines. We estimated a divergence time among the two haplogroups around 800 kya (549 - 1.259 kya HPD). Our findings showed a mismatch in subspecies assignment using morphology and genetic information and a marked differentiation between the eastern L.s. niloticus and all the other L. senator populations.

zoology↗