Agarwal Sunita K, Impey Soren, McWeeney Shannon, Scacheri Peter C, Collins Francis S, Goodman Richard H, Spiegel Allen M, Marx Stephen J
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-1802, USA.
Neoplasia. 2007 Feb;9(2):101-7. doi: 10.1593/neo.06706.
Menin is the protein product of the MEN1 tumor-suppressor gene; one allele of MEN1 is inactivated in the germ line of patients with "multiple endocrine neoplasia type 1" (MEN1) cancer syndrome. Menin interacts with several proteins involved in transcriptional regulation. RNA expression analyses have identified several menin-regulated genes that could represent proximal or distal interaction sites for menin. This report presents a substantial and unbiased sampling of menin-occupied chromatin regions using Serial Analysis of Chromatin Occupancy; this method combines chromatin immuno-precipitation with Serial Analysis of Gene Expression. Hundreds of menin-occupied genomic sites were identified in promoter regions (32% of menin-occupied loci), near the 3' end of genes (14%), or inside genes (21%), extending other data about menin recruitments to many sites of transcriptional activity. A large number of menin-occupied sites (33%) were located outside known gene regions. Additional annotation of the human genome could help in identifying genes at these loci, or these might be gene-free regions of the genome where menin occupancy could play some structural or regulatory role. Menin occupancy at many intragenic positions distant from the core promoter reveals an unexpected type of menin target region at many loci in the genome. These unbiased data also suggest that menin could play a broad role in transcriptional regulation.
Menin是MEN1肿瘤抑制基因的蛋白质产物;在“1型多发性内分泌肿瘤”(MEN1)癌症综合征患者的生殖系中,MEN1的一个等位基因失活。Menin与几种参与转录调控的蛋白质相互作用。RNA表达分析已鉴定出几个受Menin调控的基因,这些基因可能代表Menin的近端或远端相互作用位点。本报告使用染色质占据序列分析对Menin占据的染色质区域进行了大量且无偏差的抽样;该方法将染色质免疫沉淀与基因表达序列分析相结合。在启动子区域(Menin占据位点的32%)、基因3'端附近(14%)或基因内部(21%)鉴定出数百个Menin占据的基因组位点,将关于Menin募集的其他数据扩展到许多转录活性位点。大量Menin占据位点(33%)位于已知基因区域之外。对人类基因组的进一步注释可能有助于识别这些位点的基因,或者这些可能是基因组中的无基因区域,Menin占据可能在其中发挥某种结构或调节作用。Menin在许多远离核心启动子的基因内位置的占据揭示了基因组中许多位点存在一种意想不到的Menin靶区域类型。这些无偏差数据还表明Menin可能在转录调控中发挥广泛作用。