CLAN, a novel human CED-4-like gene

JS Damiano, C Stehlik, F Pio, A Godzik, JC Reed - Genomics, 2001 - Elsevier
JS Damiano, C Stehlik, F Pio, A Godzik, JC Reed
Genomics, 2001Elsevier
Proteins governing cell death form the basis of many normal processes and contribute to the
pathogenesis of many diseases when dysregulated. Here we report the cloning of a novel
human CED-4-like gene, CLAN, and several of its alternatively spliced isoforms. These
caspase-associated recruitment domain (CARD)-containing proteins are expressed at
varying degrees in normal human tissues and may contribute to a number of intracellular
processes including apoptosis, cytokine processing, and NF-κB activation. The CARD of the …
Proteins governing cell death form the basis of many normal processes and contribute to the pathogenesis of many diseases when dysregulated. Here we report the cloning of a novel human CED-4-like gene, CLAN, and several of its alternatively spliced isoforms. These caspase-associated recruitment domain (CARD)-containing proteins are expressed at varying degrees in normal human tissues and may contribute to a number of intracellular processes including apoptosis, cytokine processing, and NF-κB activation. The CARD of the CLAN proteins binds a number of other CARD-containing proteins including caspase-1, BCL10, NOD2, and NAC. Once their physiologic functions are uncovered, CLAN proteins may prove to be valuable therapeutic targets.
Elsevier