Cancer-specific rRNA variant expression is found in the TCGA dataset. By comparing cancer and control biopsies, we find cancer-specific rRNA variant expression in different cancer types, including an increase in lowly abundant rRNA variants.
Cancer-specific rRNA variant expression is found in the TCGA dataset. By comparing cancer and control biopsies, we find cancer-specific rRNA variant expression in different cancer types, including an increase in lowly abundant rRNA variants.
We discover in the GTEx dataset tissue specific rRNA variant expression levels, including rRNA variant expression level differences between brain tissues (derived from the ectoderm lineage) and digestive system tissues (derived from the endoderm lineage).
We discover in the GTEx dataset tissue specific rRNA variant expression levels, including rRNA variant expression level differences between brain tissues (derived from the ectoderm lineage) and digestive system tissues (derived from the endoderm lineage).
By structure probing full-length 28S (DMS + RIBO-RT), we find that 28S subtypes have different structures. This includes a major change in structure at the expansion segment es27l near a GGC indel variant.
By structure probing full-length 28S (DMS + RIBO-RT), we find that 28S subtypes have different structures. This includes a major change in structure at the expansion segment es27l near a GGC indel variant.
We in-situ sequence ribosomes with variations by developing a new technology, SWITCH-seq, and find that variants are co-expressed in individual cells in single-cell resolution.
We in-situ sequence ribosomes with variations by developing a new technology, SWITCH-seq, and find that variants are co-expressed in individual cells in single-cell resolution.
By full-length rRNA sequencing, RIBO-RT, we discovered ~1500 variants and tens of high-abundant variants in translating ribosomes that we curate into an atlas of human rRNA variations. Highly expressed variants are localized in eukaryotic solvent-exposed expansion segments.
By full-length rRNA sequencing, RIBO-RT, we discovered ~1500 variants and tens of high-abundant variants in translating ribosomes that we curate into an atlas of human rRNA variations. Highly expressed variants are localized in eukaryotic solvent-exposed expansion segments.
We show that Human ribosomes have different rRNA sequences, predominantly indels. These include abundant variants such as GGC indels, which form different structures. We visualize variants in single cells and associate them with development and cancer.
doi.org/10.1016/j.xgen…
We show that Human ribosomes have different rRNA sequences, predominantly indels. These include abundant variants such as GGC indels, which form different structures. We visualize variants in single cells and associate them with development and cancer.
doi.org/10.1016/j.xgen…
cell.com/cell-reports/f…
cell.com/cell-reports/f…
nature.com/articles/s4155…
nature.com/articles/s4155…
nature.com/articles/s4155…
nature.com/articles/s4155…
neurogenetics.med.ufl.edu/faculty/kotaro…
neurogenetics.med.ufl.edu/faculty/kotaro…