How mimicking the human expression of a single gene can increase neurogenesis in the developing mouse neocortex.
When the right gene is expressed in the right manner in the right population of stem cells, the developing mouse brain can exhibit primate-like features. Researchers at the Max Planck Institute of Molecular Cell Biology and Genetics succeeded in mimicking the sustained expression of the transcription factor Pax6 as seen in the developing human brain, in mouse cortical progenitor cells.
The left brain hemisphere shows the normal level and cellular distribution of Pax6 expression in the developing neocortex. The right brain hemisphere shows a sustained, primate-like Pax6 expression pattern in the neocortex of a double transgenic mouse embryo. These animals have more Pax6-positive progenitor cells and a higher Pax6 expression level in the germinal layer close to the ventricle in the right hemisphere.
© MPI of Molecular Cell Biology & Genetics
This altered the behavior of these cells to one that is akin to that of progenitors in the developing primate neocortex. Consequently, the mouse progenitors generated more neurons – a prerequisite for a bigger brain.
The developing neocortex contains different types of neural stem and progenitor cells, but one particular class, the basal progenitors, behave differently in small-brained animals such as mice than in large-brained animals such as humans. In humans, basal progenitors can undergo multiple rounds of cell division, thereby substantially increasing neuron number and ultimately the size of the neocortex.
In mice, these progenitors typically undergo only one round of cell division, thus limiting the number of neurons produced. A potential cause underlying this difference in the proliferative capacity of basal progenitors could be the differential expression of Pax6 between species. Mouse basal progenitors, in contrast to human, do not express Pax6.
“We were very curious to see what would happen if we were to change the expression pattern of Pax6 in developing mouse brain to mimic that observed in large-brained animals”, says Fong Kuan Wong, a PhD student in the lab of Wieland Huttner and first author of the study.
To this end, another PhD student in the lab, Ji-Feng Fei, generated a novel transgenic mouse line. This line provided the basis for altering the expression of Pax6 in the cortical stem cell lineage such that it would be sustained in basal progenitors. The researchers then introduced the Pax6 gene into the stem cells of these mouse embryos.
Strikingly, sustaining Pax6 expression in mouse basal progenitors increased their capacity to undergo multiple rounds of cell division, as typically observed in primates. This not only expanded the size of the basal progenitor population in a way somewhat reminiscent to what is seen in large-brained animals. It also resulted in an increase in cortical neurons, notably those in the top layer, another characteristic feature of an expanded neocortex.
“The evolutionary expansion of the neocortex is a hallmark of species with higher cognitive functions. Our findings contribute to our understanding of the molecular mechanisms underlying this expansion”, explains Wieland Huttner, the research group leader and director at the MPI-CBG. While the findings demonstrate how altering the expression of a single key gene can make a big difference to brain development, a future challenge will be to obtain a comprehensive, integrated view of all the molecular changes that made our brains big.
Prof. Dr. Wieland B. Huttner
Max Planck Institute of Molecular Cell Biology and Genetics, Dresden
Phone: +49 351 210-1500
Fax: +49 351 210-1600
Max Planck Institute of Molecular Cell Biology and Genetics, Dresden
Phone: +49 351 210-2840
Fax: +49 351 210-1019
Fong Kuan Wong, Ji-Feng Fei, Felipe Mora-Bermudez, Elena Taverna, Christiane Haffner, Jun Fu, Konstantinos Anastassiadis, A. Francis Stewart & Wieland B. Huttner
Sustained Pax6 expression generates primate-like basal radial glia in developing mouse neocortex
PLOS Biology (2015), August 6, 2015
Prof. Dr. Wieland B. Huttner | Max Planck Institute of Molecular Cell Biology and Genetics, Dresden
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