Identification and characterization of early human photoreceptor states and cell-state-specific retinoblastoma-related features
Abstract
Human cone photoreceptors differ from rods and serve as the retinoblastoma cell-of-origin, yet the developmental basis for their distinct behaviors is poorly understood. Here, we used deep full-length single-cell RNA-sequencing (scRNA-seq) to distinguish post-mitotic cone and rod developmental states and identify cone-specific features that contribute to retinoblastomagenesis. The analyses revealed nascent, immediately post-mitotic cone- and rod precursor populations characterized by higher THRB or NRL regulon activities, immature and maturing cone and rod precursors with concurrent cone- and rod-related gene and regulon expression, and distinct early and late cone and rod maturation states distinguished by maturation-associated declines in RAX regulon activity. Cell-state-specific gene expression features inferred based on full-length scRNA-seq were consistent with past single nucleus 3’ RNA-seq analyses. Beyond the cell state characterizations, full-length scRNAseq revealed that both L/M cone and rod precursors co-expressedNRLandTHRBRNAs, yet they differentially expressed functionally antagonisticNRLandTHRBisoforms and prematurely terminatedTHRBtranscripts. Moreover, early L/M cone precursors exhibited successive expression of several lncRNAs along withMYCN, which composed the seventh most L/M-cone-specific regulon, andSYK, which was implicated in the cone precursors’ proliferative response toRB1loss. These findings reveal previously unresolved photoreceptor precursor states and suggest a role for early cone-precursor-intrinsicSYKexpression in retinoblastoma initiation.
Impact Statement
Features acquired by early post-mitotic retinal cells underlie the distinct behaviors of rods and the cone cells of origin of retinoblastoma tumors.
Related articles
Related articles are currently not available for this article.