Cg-rich Genomic Loci

Cg-rich genomic loci are DNA regions with an unusually high proportion of cytosine and guanine bases, often forming regulatory landscapes that influence genome function. Their sequence composition can support CpG-rich elements, where cytosine methylation alters chromatin accessibility and transcription factor binding, thereby affecting whether nearby genes are expressed or silenced. In biology, analyzing these loci helps identify promoters, epigenetic regulatory regions, and genomic features associated with development, cellular identity, disease, and genome instability. Mapping Cg-rich regions alongside DNA methylation and gene-expression data provides insight into how sequence composition and epigenetic mechanisms cooperate to regulate gene activity.

Cg-rich Genomic Loci - Related Videos

Research

JoVE Journal - Genetics

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations

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Cited by 2 •

2021

This analytical computational platform provides practical guidance for microbiologists, ecologists, and epidemiologists interested in bacterial population genomics. Specifically, the work presented here demonstrated how to perform: i) phylogeny-guided mapping of hierarchical genotypes; ii) frequency-based analysis of genotypes; iii) kinship and clonality analyses; iv) identification of lineage differentiating accessory loci.

Education

JoVE Science Education - Advanced Biology

Genome Editing

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2023

A well-established technique for modifying specific sequences in the genome is gene targeting by homologous recombination, but this method can be laborious and only works in certain organisms. Recent advances have led to the development of “genome editing”, which works by inducing double-strand breaks in DNA using engineered nuclease enzymes guided to target genomic sites by either proteins or RNAs that recognize specific sequences. When a cell attempts to repair this damage, mutations can be...

Isolation and Genome Analysis of Single Virions using 'Single Virus Genomics'

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Cited by 2 •

2013

Single Virus Genomics (SVG) is a method to isolate and amplify the genomes of single virons. Viral suspensions of a mixed assemblage are sorted using flow cytometry onto a microscope slide with discrete wells containing agarose, thereby capturing the virion and reducing genome shearing during downstream processing. Whole genome amplification is achieved using multiple displacement amplification (MDA) resulting in genomic material that is suitable for sequencing.

Research

JoVE Journal - Biology
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Genomic MRI - a Public Resource for Studying Sequence Patterns within Genomic DNA

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Cited by 2 •

2011

We present a public computational web site for the analysis of genomic sequences. It detects DNA sequence patterns with various non-random nucleotide compositions. This resource also generates randomized sequences with diverse levels of complexity.

Research

JoVE Journal - Medicine
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Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer

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Cited by 16 •

2013

Human endogenous retroviruses (HERV), which occupy 8% of the human genome, retain scarce coding capacities but a hundred thousand long terminal repeats (LTRs). A custom Affymetrix microarray was designed to identify individual HERV locus expression and was used on prostate cancer tissues as a proof of concept for future clinical studies.

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