Researchers have united in a consortium called SSPsyGene to investigate the genetic origins of neurodevelopmental and psychiatric disorders (NPD), including schizophrenia, bipolar disorder, autism, and depression.

They are focusing on 250 high-risk genes, with the initial testing phase targeting 23 genes. The stem cell lines derived from this project will be shared with scientists worldwide to further research and treatment efforts, as published in the journal Stem Cell Reports (1^✔ ✔Trusted Source
Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs

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It’s becoming more and more clear that genetic mutations in certain genes can increase the likelihood of developing NPD, and several hundreds of those “risk genes” have been identified to date, but their role related to NPD remains a mystery.

Uniting Global Experts to Tackle NPDs

“Very little is known about the basic function of most of these genes, and what we do know often comes from work in cancer cell lines rather than brain cell types,” says David Panchision, Chief of the Developmental and Genomic Neuroscience Research Branch at the National Institute of Mental Health (NIMH), who spearheaded the SSPsyGene program aiming to tackle this challenge.

“As such, we still don’t have a clear understanding of how alterations in these genes may work individually or in combination to contribute to neurodevelopmental and psychiatric disorders.”

To get to the bottom of this, the National Institute of Mental Health (NIMH) initiated a consortium called SSPsyGene (sspsygene.ucsc.edu) in 2023, uniting research teams from renowned US universities with the joint goal of characterizing the genetic origins of NPD, focusing on 250 selected high-risk genes.

Among the contributors are Jubao Duan, Endeavor Health (formerly NorthShore University Health System) and University of Chicago, USA, and Zhiping Pang, Rutgers University, USA with their teams, who developed a method for mutating NPD risk genes in human stem cells at large scale.

In the modified cells, a selected NPD risk gene is mutated so that it no longer makes a functional protein.

The modified stem cells can subsequently be turned into neurons and other brain cells to model the consequences of risk gene mutations in a simplified, lab-based version of the human brain.

In the initial phase of the project, the teams tested 23 NPD risk genes.

The resulting stem cell lines will be made available to other researchers worldwide to facilitate research on those risk genes and their contribution to NPD.

In future works, Pang, Duan, and the other members of the consortium will join forces to generate mutated stem cell lines for a much larger number of risk genes, with the ultimate goal of understanding the genetic causes for NPD and for generating better treatments.

“The hope is that this collaborative work will generate a highly impactful resource for the neuroscience and psychiatric research community,” Panchision says.

Reference:

1. Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs
   – (https://www.cell.com/stem-cell-reports/fulltext/S2213-6711(24)00241-8)

Source-Eurekalert