Neural system-enriched gene expression: relationship to biological pathways and neurological diseases

Author:

Zhang Jianhua1,Moseley Amy2,Jegga Anil G.3,Gupta Ashima3,Witte David P.4,Sartor Maureen5,Medvedovic Mario5,Williams Sarah S.3,Ley-Ebert Cathy6,Coolen Lique M.1,Egnaczyk Gregory7,Genter Mary Beth5,Lehman Michael1,Lingrel Jerry2,Maggio John7,Parysek Linda1,Walsh Ryan1,Xu Ming1,Aronow Bruce J.36

Affiliation:

1. Departments of Cell Biology, Neurobiology and Anatomy, University of Cincinnati College of Medicine, Cincinnati 45267

2. Molecular Genetics, Microbiology and Biochemistry, University of Cincinnati College of Medicine, Cincinnati 45267

3. Division of Pediatric Informatics, Children’s Hospital Research Foundation, Cincinnati, Ohio 45229

4. Division of Pathology, Children’s Hospital Research Foundation, Cincinnati, Ohio 45229

5. Environmental Health, University of Cincinnati College of Medicine, Cincinnati 45267

6. Division of Molecular and Developmental Biology, Children’s Hospital Research Foundation, Cincinnati, Ohio 45229

7. Pharmacology and Cellular Biophysics, University of Cincinnati College of Medicine, Cincinnati 45267

Abstract

To understand the commitment of the genome to nervous system differentiation and function, we sought to compare nervous system gene expression to that of a wide variety of other tissues by gene expression database construction and mining. Gene expression profiles of 10 different adult nervous tissues were compared with that of 72 other tissues. Using ANOVA, we identified 1,361 genes whose expression was higher in the nervous system than other organs and, separately, 600 genes whose expression was at least threefold higher in one or more regions of the nervous system compared with their median expression across all organs. Of the 600 genes, 381 overlapped with the 1,361-gene list. Limited in situ gene expression analysis confirmed that identified genes did represent nervous system-enriched gene expression, and we therefore sought to evaluate the validity and significance of these top-ranked nervous system genes using known gene literature and gene ontology categorization criteria. Diverse functional categories were present in the 381 genes, including genes involved in intracellular signaling, cytoskeleton structure and function, enzymes, RNA metabolism and transcription, membrane proteins, as well as cell differentiation, death, proliferation, and division. We searched existing public sites and identified 110 known genes related to mental retardation, neurological disease, and neurodegeneration. Twenty-one of the 381 genes were within the 110-gene list, compared with a random expectation of 5. This suggests that the 381 genes provide a candidate set for further analyses in neurological and psychiatric disease studies and that as a field, we are as yet, far from a large-scale understanding of the genes that are critical for nervous system structure and function. Together, our data indicate the power of profiling an individual biologic system in a multisystem context to gain insight into the genomic basis of its structure and function.

Publisher

American Physiological Society

Subject

Genetics,Physiology

Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3