This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility:


peer-reviewed publication

trusted source


New study offers insight into genesis of spina bifida

Credit: Pixabay/CC0 Public Domain

A group of researchers at the University of California San Diego School of Medicine have led an investigation that offers new insight into the causes of spina bifida, the most common structural disorder of the human nervous system.

Work of the group, led by Keng Ioi Vong, Ph.D., and Sangmoon Lee, M.D. Ph.D., both from the laboratory of Joseph G. Gleeson, M.D., at the UC San Diego School of Medicine Department of Neurosciences and the Rady Children's Institute for Genomic Medicine, reveals the first link between and a common chromosomal microdeletion in humans. The study demonstrates that individuals carrying this chromosomal deletion—present in one of 2,500 —demonstrate a risk of spina bifida more than 10 times greater than the general public.

The study also underscores the potential role of a common food supplement in reducing the risk of spina bifida. The findings were recently published in the journal Science.

Gleeson, Rady Professor in the Department of Neuroscience and director of neuroscience at Rady Children's Institute for Genomic Medicine, is the senior author of the study. He explained that spina bifida, also known as meningomyelocele, affects one in every 3,000 newborns. Unfortunately, the causes are mostly unknown. A few mutations were reported but could only explain a tiny fraction of risk, Gleeson added.

To uncover the genetic causes of the disease, Gleeson's UC San Diego lab joined with colleagues from across the globe to establish the Spina Bifida Sequencing Consortium in 2015. The consortium began focusing on a tiny deletion in chromosome 22. Chromosome microdeletions refer to a condition in which several genes in a chromosome are missing. The group's target condition, known as 22q11.2del, has been implicated in a number of other disorders. The team began looking for 22q11.2del in spinal bifida patients.

"All patients we recruited have the most severe form of spina bifida, and all underwent best-practice comprehensive genomic sequencing," Gleeson said. "We identified 22q11.2del in 6 out of 715 patients. This may not seem a high percentage, but this is by far the most common single genetic variation that could contribute to spina bifida."

He went on to say the group identified eight additional spina bifida patients who carried the deletion from a cohort of approximately 1,500 individuals recruited because of the presence of the common 22q11.2 deletion, Gleeson said.

The researchers then narrowed the cause among the many genes in the 22q11.2 deletion to a single gene known as CRKL. Gleeson explained that there are nine other genes in this chromosomal region that could have been the cause. He said the team began a process of elimination, "knocking out" each of the mouse genes one by one, when they received a fortuitous email from Dolores Lamb from Weil Cornell College of Medicine.

Lamb had noted some of the mice in their vivarium that were missing Crkl and showed spina bifida. (Vong explained that researchers use all capital letters to describe the gene in humans, and lower-case for mice.) Lamb's group heard about the Gleeson lab project throughs the Spina Bifida Association.

"This finding really got us excited because it meant that CRKL disruption might be sufficient for spina bifida," said Vong, co-first author of the study. "We removed the mouse Crkl gene ourselves and confirmed that some of the mice developed neural tube defects, including spina bifida." Most of the other genes in 22q11.2 deletion were subsequently excluded, he added.

They next turned their attention to how might modulate CRKL-mediated spina bifida. Vong noted that prior studies in humans demonstrated that folic acid (also known as vitamin B-9) supplementation prior to conception reduces the incidence of spina bifida and other neural tube defects by up to 30–50%, but the mechanisms are still a mystery.

"When we deprived the Crkl mutant female mice of folic acid in their chow, many more of their offspring had neural tube defects, and the severity increased dramatically," Vong explained. "This suggests that folic acid taken by may not only reduce the risk, but also the severity of neural tube defects in their offspring."

"We hope our findings can help the research community to better understand causes of , especially the causes attributable to common genetic findings like 22q11.2 deletion," Gleeson said. "We also hope our findings can contribute to healthy pregnancies, improved women's health, and improved outcomes for children."

More information: Keng Ioi Vong et al, Risk of meningomyelocele mediated by the common 22q11.2 deletion, Science (2024). DOI: 10.1126/science.adl1624

Journal information: Science
Citation: New study offers insight into genesis of spina bifida (2024, May 8) retrieved 15 June 2024 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Raising awareness of spina bifida


Feedback to editors