Loss of the Polycomb group gene polyhomeotic induces non-autonomous cell overproliferation

被引:22
作者
Feng, Siqian [1 ,2 ]
Huang, Jianhua [1 ]
Wang, Jian [1 ,2 ]
机构
[1] Univ Maryland, Dept Entomol, College Pk, MD 20742 USA
[2] Univ Maryland, Biol Sci Grad Program, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
polyhomeotic; non-autonomous cell overproliferation; JAK/STAT pathway; Notch signalling; Upd homologues; DROSOPHILA JAK/STAT PATHWAY; COMPLEX; MELANOGASTER; PROTEINS; CANCER; LOCUS; VPS25; OVERGROWTH; APOPTOSIS; COMPONENT;
D O I
10.1038/embor.2010.188
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polycomb group (PcG) proteins are conserved epigenetic regulators that are linked to cancer in humans. However, little is known about how they control cell proliferation. Here, we report that mutant clones of the PcG gene polyhomeotic (ph) form unique single-cell-layer cavities that secrete three JAK/STAT pathway ligands, which in turn act redundantly to stimulate overproliferation of surrounding wild-type cells. Notably, different ph alleles cause different phenotypes at the cellular level. Although the ph-null allele induces non-autonomous overgrowth, an allele encoding truncated Ph induces both autonomous and non-autonomous overgrowth. We propose that PcG misregulation promotes tumorigenesis through several cellular mechanisms.
引用
收藏
页码:157 / 163
页数:7
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