AI Article Synopsis

  • The CTBP2/RIBEYE gene locus produces diverse isoforms crucial for retina development and helps in coding for various proteins with distinct functions.
  • Through histochemical and sequencing analyses, the study examined how CTBP2 and RIBEYE are expressed at different stages in chicken retinas, revealing CTBP2's broad presence in early developmental stages and RIBEYE's specific expression in photoreceptor cells later.
  • Comparisons between chicken and human retinal development indicate that while the regulation of the CTBP2/RIBEYE locus is similar, it involves different transcription factors in each species.

Article Abstract

Complex transcriptional gene regulation allows for multifaceted isoform production during retinogenesis, and novel isoforms transcribed from a single locus can have unlimited potential to code for diverse proteins with different functions. In this study, we explored the CTBP2/RIBEYE gene locus and its unique repertoire of transcripts that are conserved among vertebrates. We studied the transcriptional coregulator (CTBP2) and ribbon synapse-specific structural protein (RIBEYE) in the chicken retina by performing comprehensive histochemical and sequencing analyses to pinpoint cell and developmental stage-specific expression of CTBP2/RIBEYE in the developing chicken retina. We demonstrated that CTBP2 is widely expressed in retinal progenitors beginning in early retinogenesis but becomes limited to GABAergic amacrine cells in the mature retina. Inversely, RIBEYE is initially epigenetically silenced in progenitors and later expressed in photoreceptor and bipolar cells where they localize to ribbon synapses. Finally, we compared CTBP2/RIBEYE regulation in the developing human retina using a pluripotent stem cell derived retinal organoid culture system. These analyses demonstrate that similar regulation of the CTBP2/RIBEYE locus during chick and human retinal development is regulated by different members of the K50 homeodomain transcription factor family.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793361PMC
http://dx.doi.org/10.3389/fnmol.2021.773356DOI Listing

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