The histone demethylase Kdm5 controls Hid-induced cell death in Drosophila.

Frontiers in cell death Pub Date : 2024-01-01 Epub Date: 2024-11-19 DOI:10.3389/fceld.2024.1471050
Hans-Martin Herz, Andreas Bergmann
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Abstract

We conducted an EMS mutagenesis screen on chromosome arm 2L to identify recessive suppressors of GMR-hid-induced apoptosis in the Drosophila eye. Through this screen, we recovered three alleles of the lysine demethylase gene Kdm5. Kdm5, a member of the JmjC-domain-containing protein family, possesses histone demethylase activity towards H3K4me3. Our data suggest that Kdm5 specifically regulates Hid-induced cell death during development, as we did not observe control of Reaper- or Grim-induced cell death by Kdm5. Interestingly, GMR-hid-induced apoptosis is suppressed independently of Kdm5's demethylase activity. Our findings indicate that Rbf and dMyc are necessary for Kdm5 mosaics to suppress GMR-hid-induced cell death. Moreover, Kdm5 mosaics failed to suppress apoptosis induced by a mutant form of Hid that is resistant to inhibition by Erk-type MAPK activity. Additionally, Kdm5 dominantly enhances the wing phenotype of an activated MAPK mutant. These results collectively suggest that Kdm5 controls Hid-induced apoptosis by regulating the Rbf, dMyc, and MAPK pathways.

组蛋白去甲基化酶Kdm5控制hid诱导的果蝇细胞死亡。
我们对果蝇眼染色体臂2L进行了EMS诱变筛选,以鉴定gmr -hid诱导的果蝇眼细胞凋亡的隐性抑制因子。通过筛选,我们恢复了赖氨酸去甲基化酶基因Kdm5的三个等位基因。Kdm5是jmjc结构域蛋白家族的一员,具有针对H3K4me3的组蛋白去甲基化酶活性。我们的数据表明,Kdm5在发育过程中特异性调节hid诱导的细胞死亡,因为我们没有观察到Kdm5对死神或格林诱导的细胞死亡的控制。有趣的是,gmr - hide诱导的细胞凋亡被独立抑制于Kdm5的去甲基化酶活性。我们的研究结果表明,Rbf和dMyc是Kdm5嵌合抑制gmr - hid诱导的细胞死亡所必需的。此外,Kdm5嵌合体不能抑制突变型Hid诱导的细胞凋亡,而突变型Hid可抵抗erk型MAPK活性的抑制。此外,Kdm5显著增强了活化的MAPK突变体的翅膀表型。这些结果共同表明,Kdm5通过调节Rbf、dMyc和MAPK通路来控制hid诱导的细胞凋亡。
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