Lee Jungeun, He Kun, Stolc Viktor, Lee Horim, Figueroa Pablo, Gao Ying, Tongprasit Waraporn, Zhao Hongyu, Lee Ilha, Deng Xing Wang
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Conecticut 06520-8104, USA.
Plant Cell. 2007 Mar;19(3):731-49. doi: 10.1105/tpc.106.047688. Epub 2007 Mar 2.
The transcription factor LONG HYPOCOTYL5 (HY5) acts downstream of multiple families of the photoreceptors and promotes photomorphogenesis. Although it is well accepted that HY5 acts to regulate target gene expression, in vivo binding of HY5 to any of its target gene promoters has yet to be demonstrated. Here, we used a chromatin immunoprecipitation procedure to verify suspected in vivo HY5 binding sites. We demonstrated that in vivo association of HY5 with promoter targets is not altered under distinct light qualities or during light-to-dark transition. Coupled with DNA chip hybridization using a high-density 60-nucleotide oligomer microarray that contains one probe for every 500 nucleotides over the entire Arabidopsis thaliana genome, we mapped genome-wide in vivo HY5 binding sites. This analysis showed that HY5 binds preferentially to promoter regions in vivo and revealed >3000 chromosomal sites as putative HY5 binding targets. HY5 binding targets tend to be enriched in the early light-responsive genes and transcription factor genes. Our data thus support a model in which HY5 is a high hierarchical regulator of the transcriptional cascades for photomorphogenesis.
转录因子长下胚轴5(HY5)在多个光受体家族的下游发挥作用,并促进光形态建成。尽管人们普遍认为HY5可调节靶基因表达,但尚未证明HY5在体内与任何靶基因启动子的结合。在此,我们使用染色质免疫沉淀方法来验证可疑的体内HY5结合位点。我们证明,在不同的光质条件下或在光暗转换期间,HY5与启动子靶标的体内结合并未改变。结合使用高密度60核苷酸寡聚物微阵列进行的DNA芯片杂交,该微阵列在整个拟南芥基因组中每500个核苷酸包含一个探针,我们绘制了全基因组范围内的体内HY5结合位点图谱。该分析表明,HY5在体内优先与启动子区域结合,并揭示了超过3000个染色体位点作为假定的HY5结合靶标。HY5结合靶标倾向于在早期光响应基因和转录因子基因中富集。因此,我们的数据支持一种模型,即HY5是光形态建成转录级联反应的高级调节因子。