TY - JOUR
T1 - Systems biology in the central nervous system
T2 - A brief perspective on essential recent advancements
AU - Dougherty, Joseph D.
AU - Yang, Chengran
AU - Lake, Allison M.
N1 - Publisher Copyright:
© 2017 Elsevier Ltd.
PY - 2017/6
Y1 - 2017/6
N2 - As recent advances in human genetics have begun to more rapidly identify the individual genes contributing to risk of psychiatric disease, the spotlight now turns to understanding how disruption of these genes alters the brain, and thus behavior. Compared to other tissues, cellular complexity in the brain provides both a substantial challenge and a significant opportunity for systems biology approaches. Current methods are maturing that will allow for finally defining the 'parts list' for the functioning mouse and human brains, enabling new approaches to defining how the system goes awry in disorders of the CNS. However, the availability of tissue is certainly a challenge for systems biology of neuroscience, compared to systems biology of other tissues, where biopsy is feasible. This challenge is particularly notable for disorders caused by extremely rare genetic variants. Thus computational and systems biology approaches, as well as precise experimental models by way of genome editing, will play key roles in defining mechanisms for disorders, and their individual symptoms, across varied genetic etiologies. Here, we highlight recent progress in neurogenetics, postmortem genomics, cell-type specific profiling, and precision modeling toward defining mechanisms in disease.
AB - As recent advances in human genetics have begun to more rapidly identify the individual genes contributing to risk of psychiatric disease, the spotlight now turns to understanding how disruption of these genes alters the brain, and thus behavior. Compared to other tissues, cellular complexity in the brain provides both a substantial challenge and a significant opportunity for systems biology approaches. Current methods are maturing that will allow for finally defining the 'parts list' for the functioning mouse and human brains, enabling new approaches to defining how the system goes awry in disorders of the CNS. However, the availability of tissue is certainly a challenge for systems biology of neuroscience, compared to systems biology of other tissues, where biopsy is feasible. This challenge is particularly notable for disorders caused by extremely rare genetic variants. Thus computational and systems biology approaches, as well as precise experimental models by way of genome editing, will play key roles in defining mechanisms for disorders, and their individual symptoms, across varied genetic etiologies. Here, we highlight recent progress in neurogenetics, postmortem genomics, cell-type specific profiling, and precision modeling toward defining mechanisms in disease.
KW - MPRA
KW - Postmortem transcriptome
KW - Single cell
KW - Systems molecular neuroscience
UR - http://www.scopus.com/inward/record.url?scp=85042237397&partnerID=8YFLogxK
U2 - 10.1016/j.coisb.2017.04.011
DO - 10.1016/j.coisb.2017.04.011
M3 - Review article
C2 - 29057378
AN - SCOPUS:85042237397
SN - 2452-3100
VL - 3
SP - 67
EP - 76
JO - Current Opinion in Systems Biology
JF - Current Opinion in Systems Biology
ER -