MeCP2 involvement in the regulation of neuronal α-tubulin production

Liron Abuhatzira, Ruth Shemer, Aharon Razin*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations


Rett syndrome (RTT) is a severe neurodevelopmental disorder caused by a dominant mutation in the X-linked methyl CpG binding protein 2 (MeCP2) gene. Neuroanatomically, RTT is characterized by a reduction in dendritic arborization and perikaryal size in the brain. MECP2 binds methylated promoters and facilitates assembly of a multiprotein repressor complex that includes Sin3A and the histone deacetylases HDAC1/ HDAC2. MeCP2 has recently been found to be downregulated in autistic spectrum disorders such as Angelman syndrome (AS) and RTT, which share some phenotypic manifestations. We have conducted expression analysis of cytoskeleton-related genes in brain tissue of RTT and AS patients. Striking examples of genes with reduced expression were TUBA1B and TUBA3 that encode the ubiquitous α-tubulin and the neuronal specific α-tubulin, respectively. In accordance with the downregulation of expression of these genes, we have observed a reduction in the level of the corresponding protein product-tyrosinated α-tubulin. Low levels of α-tubulin and deteriorated cell morphology were also observed in MeCP2-/y MEF cells. The effects of MeCP2 deficiency in these cells were completely reversed by introducing and expressing the human MeCP2 gene. These results imply that MeCP2 is involved in the regulation of neuronal α-tubulin and add molecular evidence that reversal of the effects of MeCP2 deficiency is achievable. This raises hopes for a cure of Rett syndrome and related MeCP2 deficiency disorders of the autistic spectrum.

Original languageAmerican English
Pages (from-to)1415-1423
Number of pages9
JournalHuman Molecular Genetics
Issue number8
StatePublished - 2009

Bibliographical note

Funding Information:
This work was supported by the Israel Science Foundation (Grant no. 104/06) and the March of Dimes Birth Defects Foundation for Inborn Disease in the USA (Grant no. 06-FY05-71).


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