AI Article Synopsis

  • CLDN18.2 is a highly conserved tight junction protein specific to gastric cells across multiple mammalian species, including humans, monkeys, and dogs.
  • The study highlights similarities in the molecular structure and regulatory elements, particularly the promoter region associated with the transcription factor CREB, which are maintained across species.
  • These findings suggest that CLDN18.2 is a promising target for drug development, indicating that the studied mammals can serve as effective models for evaluating the safety of therapies targeting this protein.

Article Abstract

Claudin-18 isoform 2 (CLDN18.2) is one of the few members of the human claudin family of tight junction molecules with strict restriction to one cell lineage. The objective of the current study was to compare molecular structure and tissue distribution of this gastrocyte specific molecule in mammals. We show here that the CLDN18.2 protein sequence is highly conserved, in particular with regard to functionally relevant domains in mouse, rat, rabbit, dog, monkey and human and also in lizards. Moreover, promoter regions of orthologs are highly homologous, including the binding site of the transcription factor cyclic AMP-responsive element binding protein (CREB), which is known to regulate activation of human CLDN18.2. Employing RT-PCR and immunohistochemistry, we found that, analogous to the human gene, all orthologous CLDN18.2 transcripts and proteins are exclusively expressed in differentiated gastric cells. Gene structure, promoter elements and RNA expression pattern of the lung-tissue specific Claudin-18 isoform 1 (CLDN18.1) as well, are homologous across species. These findings exemplify phylogenetic conservation of lineage-specific members of a multigene family. Given that CLDN18.2 is a novel drug target candidate, our data is also relevant for drug development as it reveals all six investigated mammalian species as suitable models for testing safety of CLDN18.2 targeting regimen.

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Source
http://dx.doi.org/10.1016/j.gene.2011.04.007DOI Listing

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