posted on 2016-02-20, 02:43authored byQuanhui Wang, Bo Wen, Guangrong Yan, Junying Wei, Liqi Xie, Shaohang Xu, Dahai Jiang, Tingyou Wang, Liang Lin, Jin Zi, Ju Zhang, Ruo Zhou, Haiyi Zhao, Zhe Ren, Nengrong Qu, Xiaomin Lou, Haidan Sun, Chaoqin Du, Chuangbin Chen, Shenyan Zhang, Fengji Tan, Youqi Xian, Zhibo Gao, Minghui He, Longyun Chen, Xiaohang Zhao, Ping Xu, Yunping Zhu, Xingfeng Yin, Huali Shen, Yang Zhang, Jing Jiang, Chengpu Zhang, Liwei Li, Cheng Chang, Jie Ma, Guoquan Yan, Jun Yao, Haojie Lu, Wantao Ying, Fan Zhong, Qing-Yu He, Siqi Liu
Under the guidance of the Chromosome-centric Human Proteome
Project (C-HPP),, we conducted a systematic survey
of the expression status of genes located at human chromosome 20 (Chr.20)
in three cancer tissues, gastric, colon, and liver carcinoma, and
their representative cell lines. We have globally profiled proteomes
in these samples with combined technology of LC–MS/MS and acquired
the corresponding mRNA information upon RNA-seq and RNAchip. In total,
323 unique proteins were identified, covering 60% of the coding genes
(323/547) in Chr.20. With regards to qualitative information of proteomics,
we overall evaluated the correlation of the identified Chr.20 proteins
with target genes of transcription factors or of microRNA, conserved
genes and cancer-related genes. As for quantitative information, the
expression abundances of Chr.20 genes were found to be almost consistent
in both tissues and cell lines of mRNA in all individual chromosome
regions, whereas those of Chr.20 proteins in cells are different from
tissues, especially in the region of 20q13.33. Furthermore, the abundances
of Chr.20 proteins were hierarchically evaluated according to tissue-
or cancer-related distribution. The analysis revealed several cancer-related
proteins in Chr.20 are tissue- or cell-type dependent. With integration
of all the acquired data, for the first time we established a solid
database of the Chr.20 proteome.