Publications by authors named "Samuele M Amante"

The placenta is a fast-evolving organ with large morphological and histological differences across eutherians, but the genetic changes driving placental evolution have not been fully elucidated. Transposable elements, through their capacity to quickly generate genetic variation and affect host gene regulation, may have helped to define species-specific trophoblast gene expression programs. Here we assess the contribution of transposable elements to human trophoblast gene expression as enhancers or promoters.

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Dopa decarboxylase (DDC) synthesizes serotonin in the developing mouse heart where it is encoded by , a tissue-specific paternally expressed imprinted gene. shares an imprinting control region (ICR) with the imprinted, maternally expressed (outside of the central nervous system) gene on mouse chromosome 11, but little else is known about the tissue-specific imprinted expression of . Fluorescent immunostaining localizes DDC to the developing myocardium in the pre-natal mouse heart, in a region susceptible to abnormal development and implicated in congenital heart defects in human.

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Article Synopsis
  • Alternative splicing (AS) and alternative polyadenylation (APA) create diverse transcripts in mammals, influenced by epigenetic marks like H3K36me3 and DNA methylation during development and differentiation.* -
  • The study reveals that H3K36me3 is not a key regulator of AS or APA, while identifying over 4000 host genes with intragenic CpG islands (iCGIs). These iCGIs show dynamic transcriptional activity depending on tissue and developmental stages.* -
  • It highlights that iCGI transcription affects host gene transcription and pre-mRNA processing more significantly than H3K36me3 or DNA methylation, driving diverse transcript and protein expression across different times and
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DNA binding factors are essential for regulating gene expression. CTCF and cohesin are DNA binding factors with central roles in chromatin organization and gene expression. We determined the sites of CTCF and cohesin binding to DNA in mouse brain, genome wide and in an allele-specific manner with high read-depth ChIP-seq.

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