Temasek Life Sciences Laboratory, National University of Singapore, Singapore.
PLoS Biol. 2009 Nov;7(11):e1000251. doi: 10.1371/journal.pbio.1000251. Epub 2009 Nov 24.
The Arabidopsis homeotic protein AGAMOUS (AG), a MADS domain transcription factor, specifies reproductive organ identity during flower development. Using a binding assay and expression analysis, we identified a direct target of AG, GIANT KILLER (GIK), which fine-tunes the expression of multiple genes downstream of AG. The GIK protein contains an AT-hook DNA binding motif that is widely found in chromosomal proteins and that binds to nuclear matrix attachment regions of DNA elements. Overexpression and loss of function of GIK cause wide-ranging defects in patterning and differentiation of reproductive organs. GIK directly regulates the expression of several key transcriptional regulators, including ETTIN/AUXIN RESPONSE FACTOR 3 (ETT/ARF3) that patterns the gynoecium, by binding to the matrix attachment regions of target promoters. Overexpression of GIK causes a swift and dynamic change in repressive histone modification in the ETT promoter. We propose that GIK acts as a molecular node downstream of the homeotic protein AG, regulating patterning and differentiation of reproductive organs through chromatin organization.
拟南芥同源异型蛋白 AGAMOUS(AG),一种 MADS 结构域转录因子,在花发育过程中指定生殖器官的身份。通过结合测定和表达分析,我们鉴定了 AG 的一个直接靶标 GIANT KILLER(GIK),它微调了 AG 下游多个基因的表达。GIK 蛋白含有一个 AT 钩 DNA 结合基序,该基序广泛存在于染色体蛋白中,并与 DNA 元件的核基质附着区结合。GIK 的过表达和功能丧失导致生殖器官的模式形成和分化出现广泛缺陷。GIK 通过与靶启动子的基质附着区结合,直接调节几个关键转录调节剂的表达,包括决定雌蕊模式的 ETTIN/AUXIN RESPONSE FACTOR 3(ETT/ARF3)。GIK 的过表达导致 ETT 启动子中抑制性组蛋白修饰的迅速和动态变化。我们提出,GIK 作为同源异型蛋白 AG 的下游分子节点,通过染色质组织调节生殖器官的模式形成和分化。