MicroRNA helps unravel mystery of Rett protein (MeCP2)


HOUSTON -- (February 22, 2013) -- A snippet of genetic material called microRNA provides new insight into the control of the protein MeCP2, which causes disease when there is too much or too little of it in the brain, said researchers at Baylor College of Medicine and the Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital in a report in the journal Genes and Development.

"We know that MeCP2 is important for neurological function," said Dr. Huda Zoghbi, director of the NRI and professor of molecular and human genetics at BCM. "We also know that precise control of the levels of MeCP2 in the brain is crucial to neurological function."

Zoghbi first found the gene for the protein in 1999, identifying mutations in the gene MECP2 as the cause of Rett syndrome, a post natal genetic disorder that affects mainly girls and occurs when there is too little of the protein.

In this report, Zoghbi, who is also a Howard Hughes Medical Institute investigator, and her colleagues describe a microRNA known as miR-483-5p that plays an important role in regulating the levels of MeCP2 protein in the fetal brain during development. Such microRNAs are known to affect the ability of messenger RNA (a form of genetic material) to convey the blueprint for a protein from the DNA in the nucleus to the protein-making machinery of the cell. It accomplishes this control through interaction with the 3' untranslated region (3'UTR) that flanks one side of a gene.

High levels of the microRNA (miR-483-5p) mean low levels of MeCP2, which is the state that exists in the fetal brain, said Dr. Vincenzo Gennarino, a postdoctoral associate in the Zoghbi lab. Vincenzo found that this particular microRNA interacts with the long 3'UTR found in fetal brains but not the shorter 3'UTR that is found in the brain after birth.

"Surprisingly, we have found that the binding site of miR-483-5p to the gene MECP2 is specific to humans," said Dr. Kihoon Han, a postdoctoral associate in the Zoghbi lab. They also found that the microRNA regulates levels of two proteins that interact with MeCP2, which further enhances its level of control.

"More broadly, miR-483-5p-mediated regulation of the levels of MeCP2 and some of its interacting proteins uncover an interesting example of a regulatory posttranscriptional (between the transcription of DNA to messenger RNA and the transport of that message to protein-making machinery of the cell) control of a group of genes that are functionally associated through a specific microRNA. The odds are this regulatory mechanism involves many other genes that function together and/or that express 3'UTRs in a developmental or tissue specific pattern," said Zoghbi.

Others who took part in this work include: Kihoon Han and Vincenzo Alessandro Gennarino, (who contributed equally as first authors), Yoontae Lee, Kaifang Pang and Zhandong Liu, all of BCM and the Neurological Institute; Kazue Hashimoto-Torii and Pasko Rakic of Yale University School of Medicine in New Haven, Connecticut; Sanaa Choufani and Rosanna Weksberg of The Hospital for Sick Children in Toronto, Ontario, Canada; Chandrasekhar S. Raju and Michael C. Oldham of the University of California San Francisco. Zoghbi is also a professor of pediatrics and neuroscience at BCM.

Funding for this work came from the Howard Hughes Medical Institute, the National Institutes of Health (Grant 5R01NS057819), the Baylor Intellectual and Developmental Disabilities Research Center (P30HD024064), the Administrative and Confocal cores from the Eunice Kennedy Shriver National Institute of Child Health and Human Development and the Wenner-Gren Foundations in Sweden.

For more information on research at Baylor College of Medicine, please go to www.bcm.edu/fromthelab.

About Texas Children’s Hospital

Texas Children’s Hospital, a not-for-profit health care organization, is committed to creating a healthier future for children and women throughout the global community by leading in patient care, education and research. Consistently ranked as the best children’s hospital in Texas, and among the top in the nation, Texas Children’s has garnered widespread recognition for its expertise and breakthroughs in pediatric and women’s health. The hospital includes the Jan and Dan Duncan Neurological Research Institute; the Feigin Center for pediatric research; Texas Children’s Pavilion for Women, a comprehensive obstetrics/gynecology facility focusing on high-risk births; Texas Children’s Hospital West Campus, a community hospital in suburban West Houston; and Texas Children’s Hospital The Woodlands, a second community hospital planned to open in 2017. The organization also created the nation’s first HMO for children, has the largest pediatric primary care network in the country and a global health program that’s channeling care to children and women all over the world. Texas Children’s Hospital is affiliated with Baylor College of Medicine. For more information, go to www.texaschildrens.org. Get the latest news by visiting the online newsroom and Twitter at twitter.com/texaschildrens.