Luedi Philippe P, Dietrich Fred S, Weidman Jennifer R, Bosko Jason M, Jirtle Randy L, Hartemink Alexander J
Center for Bioinformatics and Computational Biology, Duke University, Durham, North Carolina 27708, USA.
Genome Res. 2007 Dec;17(12):1723-30. doi: 10.1101/gr.6584707. Epub 2007 Nov 30.
Imprinted genes are essential in embryonic development, and imprinting dysregulation contributes to human disease. We report two new human imprinted genes: KCNK9 is predominantly expressed in the brain, is a known oncogene, and may be involved in bipolar disorder and epilepsy, while DLGAP2 is a candidate bladder cancer tumor suppressor. Both genes lie on chromosome 8, not previously suspected to contain imprinted genes. We identified these genes, along with 154 others, based on the predictions of multiple classification algorithms using DNA sequence characteristics as features. Our findings demonstrate that DNA sequence characteristics, including recombination hot spots, are sufficient to accurately predict the imprinting status of individual genes in the human genome.
印记基因在胚胎发育中至关重要,而印记调控异常会导致人类疾病。我们报告了两个新的人类印记基因:KCNK9主要在大脑中表达,是一种已知的癌基因,可能与双相情感障碍和癫痫有关,而DLGAP2是膀胱癌肿瘤抑制候选基因。这两个基因都位于8号染色体上,此前并未怀疑该染色体含有印记基因。我们基于以DNA序列特征为特征的多种分类算法的预测,鉴定出了这两个基因以及其他154个基因。我们的研究结果表明,包括重组热点在内的DNA序列特征足以准确预测人类基因组中单个基因的印记状态。