AI Article Synopsis

  • During development, out of 1090 somatic cells generated, 131 undergo apoptosis, primarily regulated by the BH3-only gene, which activates cell death in specific lineages.
  • The expression of this gene is controlled both transcriptionally and post-transcriptionally, with miR-35 and miR-58 miRNAs helping to repress it in cases of 'unwanted' cells.
  • Through identifying RNA-binding proteins like EIF-3.H and HRPR-1 as potential activators of the gene, the study shows that knocking down these genes leads to the survival of undesired cells, illuminating how cell death patterns are established in development.

Article Abstract

During development, 1090 somatic cells are generated of which 131 reproducibly die, many through apoptosis. The BH3-only gene is the key activator of apoptosis in somatic tissues, and it is predominantly expressed in 'cell death' lineages i.e. lineages in which apoptotic cell death occurs. expression is regulated at the transcriptional and post-transcriptional level. For example, we previously showed that the miR-35 and miR-58 families of miRNAs repress expression in mothers of 'unwanted' cells by binding to the 3' UTR of mRNA, thereby increasing mRNA turnover. In a screen for RNA-binding proteins with a role in the post-transcriptional control of expression, we identified EIF-3.H (ortholog of human eIF3H) and HRPR-1 (ortholog human hnRNP R/Q) as potential activators of expression. In addition, we demonstrate that the knockdown of the or gene by RNA-mediated interference (RNAi) results in the inappropriate survival of unwanted cells during development. Our study provides novel insight into how expression is controlled to cause the reproducible pattern of cell death observed during development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10905296PMC
http://dx.doi.org/10.17912/micropub.biology.001126DOI Listing

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