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Regulatory element copy number differences shape primate expression profiles

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TLDR
It is postulate that CNDs of these conserved sequences fine-tune developmental pathways by altering the levels of RNA.
Abstract
Gene expression differences are shaped by selective pressures and contribute to phenotypic differences between species. We identified 964 copy number differences (CNDs) of conserved sequences across three primate species and examined their potential effects on gene expression profiles. Samples with copy number different genes had significantly different expression than samples with neutral copy number. Genes encoding regulatory molecules differed in copy number and were associated with significant expression differences. Additionally, we identified 127 CNDs that were processed pseudogenes and some of which were expressed. Furthermore, there were copy number-different regulatory regions such as ultraconserved elements and long intergenic noncoding RNAs with the potential to affect expression. We postulate that CNDs of these conserved sequences fine-tune developmental pathways by altering the levels of RNA.

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Pseudogenes: newly discovered players in human cancer.

Laura Poliseno
- 18 Sep 2012 - 
TL;DR: Advances in the understanding of the functions of pseudogenes that have established them as versatile regulators of gene expression and key players in the pathogenesis of human cancer are summarized.
Journal ArticleDOI

Co-binding by YY1 identifies the transcriptionally active, highly conserved set of CTCF-bound regions in primate genomes

TL;DR: Combined analysis of CTCF and YY1 binding in lymphoblastoid cell lines from seven primates, as well as in mouse and human livers, reveals extensive genome-wide co-localization specifically at evolutionarily stable C TCF-bound regions.
Journal ArticleDOI

Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility

Wesley C. Warren, +62 more
- 18 Dec 2020 - 
TL;DR: A new reference genome for the rhesus macaque, a model nonhuman primate, in which most gaps were closed and most protein-coding genes were annotated is generated, improving gene mapping for biomedical and comparative genetic studies.
Journal ArticleDOI

Single-cell copy number variant detection reveals the dynamics and diversity of adaptation.

TL;DR: This study developed a fluorescent CNV reporter to detect de novo gene amplifications and deletions in individual cells and found that under strong selection, GAP1 CNVs are repeatedly generated and selected during the early stages of adaptive evolution, resulting in predictable dynamics.
References
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Journal ArticleDOI

The Human Genome Browser at UCSC

TL;DR: A mature web tool for rapid and reliable display of any requested portion of the genome at any scale, together with several dozen aligned annotation tracks, is provided at http://genome.ucsc.edu.
Book

Evolution by gene duplication

Susumu Ohno
Journal ArticleDOI

A ceRNA Hypothesis: The Rosetta Stone of a Hidden RNA Language?

TL;DR: It is proposed that this "competing endogenous RNA" (ceRNA) activity forms a large-scale regulatory network across the transcriptome, greatly expanding the functional genetic information in the human genome and playing important roles in pathological conditions, such as cancer.
Journal ArticleDOI

PAML: a program package for phylogenetic analysis by maximum likelihood

TL;DR: The strength of PAML, in comparison with other phylogenetic packages currently available, is its implementation of a variety of evolutionary models, which include several models of variable evolutionary rates among sites, models for combined analyses of multiple gene sequence data and models for amino acid sequences.
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