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The arrangement of human retinal cell chromatin, the fibres that wrap 3 billion nucleotide-long DNA molecules into compact structures that fit into chromosomes within each cell's nucleus, was mapped by National Eye Institute researchers. The resultant complete gene regulatory network sheds light on gene expression regulation in general, as well as retinal function in both unusual and prevalent eye illnesses.
The findings of the study were published in the journal Nature Communications. "This is the first detailed integration of retinal regulatory genome topology with genetic variants associated with age-related macular degeneration (AMD) and glaucoma, two leading causes of vision loss and blindness," said the study's lead investigator, Anand Swaroop, Ph.D., senior investigator and chief of the Neurobiology Neurodegeneration and Repair Laboratory at the NEI, part of the National Institutes of Health. Adult human retinal cells are highly specialized sensory neurons that do not divide and are therefore relatively stable for exploring how the chromatin's three-dimensional structure contributes to the expression of genetic information. Chromatin fibers package long strands of DNA spooled around histone proteins and then repeatedly looped to form highly compact structures. All those loops create multiple contact points where genetic sequences that code for proteins interact with gene regulatory sequences, such as super-enhancers, promoters, and transcription factors. Such non-coding sequences were long considered "junk DNA." But more advanced studies demonstrate how these sequences control which genes get transcribed and when, shedding light on the mechanisms by which non-coding regulatory elements exert control even when their location on a DNA strand is remote from the genes they regulate. Using deep Hi-C sequencing, a tool used for studying 3D genome organization, the researchers created a high-resolution map that included 704 million contact points within retinal cell chromatin. Maps were constructed using post-mortem retinal samples from four human donors. The researchers then integrated that chromatin topology map with datasets on retinal genes and regulatory elements. What emerged was a dynamic picture of interactions within chromatin over time, including gene activity hot spots and areas with varying degrees of insulation from other regions of DNA. They found distinct patterns of interaction at retinal genes suggesting how chromatin's 3D organization plays a vital role in tissue-specific gene regulation. "Having such a high-resolution picture of genomic architecture will continue to provide insights into the genetic control of tissue-specific functions," Swaroop said. Furthermore, similarities between mice and human chromatin organization suggest conservation across species, underscoring the relevance of chromatin organizational patterns for retinal gene regulation. More than a third (35.7%) of gene pairs interacting through a chromatin loop in mice also did so in the human retina. The researchers integrated the chromatin topology map with data on genetic variants identified from genome-wide association studies for their involvement in AMD and glaucoma, two leading causes of vision loss and blindness. The findings point to specific candidate causal genes involved in those diseases. The integrated genome regulatory map will also assist in evaluating genes associated with other common retina-associated diseases such as diabetic retinopathy, determining missing heritability and understanding genotype-phenotype correlations in inherited retinal and macular diseases. (ANI)
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