Scientists at St. Jude Children’s Research Hospital studied the Vsx2 super-enhancer and its role in the development of the retina. Their assessment showed the super-enhancer has four distinct regions with different functions. Moreover, this modular super-enhancer provides a way to study gene expression during development. The team has published a paper (“Identification of a modular super-enhancer in murine retinal development”) in Nature Communications.
“Super-enhancers are expansive regions of genomic DNA comprised of multiple putative enhancers that contribute to the dynamic gene expression patterns during development. This is particularly important in neurogenesis because many essential transcription factors have complex developmental stage– and cell–type specific expression patterns across the central nervous system,” write the investigators.
In the developing retina, Vsx2 is expressed in retinal progenitor cells and is maintained in differentiated bipolar neurons and Müller glia. A single super-enhancer controls this complex and dynamic pattern of expression. Here we show that deletion of one region disrupts retinal progenitor cell proliferation but does not affect cell fate specification.
“The deletion of another region has no effect on retinal progenitor cell proliferation but instead leads to a complete loss of bipolar neurons. This prototypical super-enhancer may serve as a model for dissecting the complex gene expression patterns for neurogenic transcription factors during development. Moreover, it provides a unique opportunity to alter expression of individual transcription factors in particular cell types at specific stages of development.
“This provides a deeper understanding of function that cannot be achieved with traditional knockout mouse approaches.”
The transcription factor Vsx2, which is essential to proper eye development, is expressed in retinal progenitor cells and found in established bipolar neurons and Müller glia. For decades, researchers studied Vsx2 to understand how it affects development. Gene function is typically studied by knocking out the gene and observing what changes. However, when Vsx2 is knocked out, the eye does not form. Researchers cannot study something that does not form, so they needed the ability to fine-tune Vsx2 expression, at different times during retina formation.
“In brain development, important transcription factors, like Vsx2, and many others, are often expressed in different parts of the developing brain at different times but in a precisely orchestrated way,” said corresponding author Michael Dyer, PhD, St. Jude Department of Developmental Neurobiology chair and Howard Hughes Medical Institute Investigator. “We wanted to better understand how this complicated dance of expression is controlled where the gene is turned on at one moment in one cell type, then turned off in another and later activated in a different region completely.”
Testing the first modular super-enhancer
A super-enhancer of Vsx2 controls the complex and dynamic pattern of expression involved in retinal development.
“While thousands of super-enhancers have been computationally identified, very few have been functionally tested,” said first author Victoria Honnell, a student in the St. Jude Graduate School of Biomedical Sciences. “Our functional tests of the Vsx2 super-enhancer showed distinct regions. We’ve called this a modular super-enhancer. One piece of this super-enhancer plays a role in early retinal development, and then another portion is important for bipolar cell genesis in later development.”
The scientists found four distinct regions in the Vsx2 super-enhancer. Three of these regions were involved in retinal development. This is the first-time researchers have demonstrated independent functions of distinct regions within a super-enhancer.
Studying modular super-enhancers provides more clarity regarding the functional effects of gene expression than traditional genomic approaches like knocking out the gene. Modular super-enhancers allow scientists to alter expression of individual transcription factors in particular cell types at specific stages of development. Thus, the modular super-enhancer concept may serve as a model for studying the complex gene expression patterns that occur during brain development.
“When you can fully understand how one of these modular super-enhancers works, you can go globally to all the super-enhancers with a framework to understand them more broadly,” Dyer said. “Imagine a clock that you take apart to figure out which pieces go where and what they do. If you take apart a totally different clock, you’ll already have a good blueprint for which pieces go where based on the first one.”
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