Huntington’s Gene Enhances Early Brain Growth and Intelligence

Summary: A study reveals that the genetic mutation causing Huntington’s disease (HD) enhances brain development and intelligence in early life, but leads to degeneration in adulthood. Children with the HD gene exhibit larger brains and higher IQs than those without the mutation.

This finding supports the theory of antagonistic pleiotropy, where genetic traits benefit early life but incur costs later. Researchers suggest that treatments should focus on slowing brain aging rather than silencing the HD gene. This discovery could reshape understanding of HD pathology and contribute to targeted therapies. The study also highlights the gene’s evolutionary role in brain complexity and intelligence.

Key Facts:

  • The HD mutation increases brain volume and IQ in children but leads to degeneration in adulthood.
  • The gene expansion aligns with evolutionary theories, enhancing brain complexity early in life.
  • Future therapies may benefit from targeting aging processes rather than suppressing the gene.

Source: University of Iowa

The genetic mutation that causes Huntington’s disease (HD) – a devastating brain disease that disrupts mobility and diminishes cognitive ability – may also enhance early brain development and play a role in promoting human intelligence.  

This revelation comes from more than 10 years of brain imaging and brain function data, including motor, cognitive, and behavioral assessments, collected from a unique population – children and young adults who carry the gene for HD.

This shows a pregnant woman and DNA.
The new data about the gene’s positive effect on early brain development is also exciting to Nopoulos for another reason. Credit: Neuroscience News

While an HD mutation will eventually cause fatal brain disease in adulthood, the study finds that early in life, children with the HD mutation have bigger brains and higher IQ than children without the mutation.   

“The finding suggests that early in life, the gene mutation is actually beneficial to brain development, but that early benefit later becomes a liability,” says Peg Nopoulos, MD, professor and head of psychiatry at the UI Carver College of Medicine, and senior author on the study published in The Annals of Neurology

The finding may also have implications for developing effective treatments for HD. If the gene’s early action is beneficial, then simply aiming to knock out the gene might result in loss of the developmental benefit, too. Creating therapies that can disrupt the gene’s activity later in the patient’s lifetime might be more useful. 

The new data about the gene’s positive effect on early brain development is also exciting to Nopoulos for another reason. 

“We are very interested in the fact that this appears to be a gene that drives IQ,” she says. “No previous study has found any gene of significant effect on IQ, even though we know intelligence is heritable.” 

HD gene linked to better brain development in early life 

Huntington’s disease is caused by a mutation in the huntingtin (HTT) gene. The protein produced by the HTT gene is necessary for normal development, but variations within a segment of the protein have a profound effect on the brain. 

The segment in question is a long repeat of one amino acid called glutamine. More repeats are associated with bigger, more complex brains. For example, species such as sea urchins or fish have no repeats, but these repeats start to appear higher up the evolutionary ladder.

Rodents have a few repeats, while apes (our closest relatives) have even more repeats; and humans have the most. 

Most people have repeats in the range of 10-26, but if a person has 40 or more repeats, then they develop HD. Although the gene expansion is present before birth, HD symptoms do not appear until middle age.

Nopoulos’s team at the University of Iowa has a long history of studying how the HTT gene expansion affects brain development in the decades before disease onset. 

“We know that the expanded gene causes a horrible degenerative disease later in life, but we also know it is a gene that is crucial for general development,” she says.

“We were surprised to find that it does have a positive effect on brain development early in life. Those who have the gene expansion have an enhanced brain with larger volumes of the cerebrum and higher IQ compared to those who don’t.” 

In particular, the study found that decades before HD symptoms appeared, children with the HD gene expansion showed significantly better cognitive, behavioral, and motor scores compared to children with repeats within the normal range.

Children with the expanded gene also had larger cerebral volumes and greater cortical surface area and folding. After this initial peak, a prolonged deterioration was seen in both brain function and structure. 

The study gathered this data by following almost 200 participants in the Kids-HD study, the only longitudinal study of children and young adults at risk for HD due to having a parent or grandparent with the disease. 

Evolutionary benefit comes at a cost 

Although surprising, the findings are in line with studies from evolutionary biologists who believe that genes like HTT may have been ‘positively selected’ for human brain evolution. This theory, known as antagonistic pleiotropy, suggests that certain genes can produce a beneficial effect early in life, but come at a cost later in life. 

The finding also challenges the idea that the protein produced by the HD gene is solely a toxic protein that causes brain degeneration. 

“Overall, our study suggests that we should rethink the notion of the toxic protein theory,” says Nopoulos who also is a member of the Iowa Neuroscience Institute.

“Instead, we should consider the theory of antagonistic pleiotropy – a theory that suggests that genes like HTT build a better brain early in life, but the cost of the superior brain is that it isn’t built to last and may be prone to premature or accelerating aging. 

“This means that instead of knocking down the gene for therapy, drugs that slow the aging process may be more effective.” 

Next steps 

Nopoulos’s team is already making progress extending the research from the Kids-HD program. Using a major grant received in 2019, Nopoulos established the Children to Adult Neurodevelopment in Gene-Expanded Huntington’s Disease (ChANGE-HD), a multi-site study that aims to recruit hundreds of participants for a total of over 1,200 assessments to validate the key findings from the Kids-HD study and to enhance future research on HD. 

A primary area of focus will be understanding how an enlarged brain can later lead to degeneration. One hypothesis Nopoulos and her team will explore involves the idea that an enlarged cortex might produce excess glutamate (an important neurotransmitter), which is beneficial in early brain development, but later leads to neurotoxicity and brain degeneration.  

In addition to Nopoulos, the UI team included Mohit Neema, MD, UI research scientist and first author of the study; Jordan Schultz, PharmD; Douglas Langbehn, MD, PhD; Amy Conrad, PhD; Eric Epping, MD, PhD; and Vincent Magnotta PhD. 

Funding: The research was funded in part by grants from the National Institute of Neurological Disorders and Stroke and the CHDI Foundation. 

About this genetics and neurodevelopment research news

Author: Jennifer Brown
Source: University of Iowa
Contact: Jennifer Brown – University of Iowa
Image: The image is credited to Neuroscience News

Original Research: Open access.
Mutant Huntingtin Drives Development of an Advantageous Brain Early in Life: Evidence in Support of Antagonistic Pleiotropy” by Peg Nopoulos et al. Annals of Neurology


Abstract

Mutant Huntingtin Drives Development of an Advantageous Brain Early in Life: Evidence in Support of Antagonistic Pleiotropy

Objective

Huntington’s disease (HD) is a neurodegenerative disease caused by a triplet repeat expansion within the gene huntingtin (HTT). Antagonistic pleiotropy is a theory of aging that posits that some genes, facilitating individual fitness early in life through adaptive evolutionary changes, also augment detrimental aging-related processes.

Antagonistic pleiotropy theory may explain a positive evolutionary pressure toward functionally advantageous brain development that is vulnerable to rapid degeneration. The current study investigated antagonistic pleiotropy in HD using a years-to-onset paradigm in a unique sample of children and young adults at risk for HD.

Methods

Cognitive, behavioral, motor, and brain structural measures from premanifest gene-expanded (n = 79) and gene nonexpanded (n = 112) participants (6–21 years) in the Kids-HD study were examined. All measures in the gene-expanded group were modeled using a mixed-effects regression approach to assess years-to-onset-based changes while controlling for normal growth. Simultaneously, structure–function associations were also examined.

Results

Decades from motor onset, gene-expanded participants showed significantly better cognitive, behavioral, and motor scores versus gene nonexpanded controls, along with larger cerebral volumes and cortical features. After this initial peak, a prolonged deterioration was observed in both functional and structural measures.

Far from onset, brain measures were positively correlated with functional measures, supporting the view that functional advantages were mediated by structural differences.

Interpretation

Mutant HTT may drive the development of a larger than normal brain that subserves superior early-life function. These findings support the antagonistic pleiotropy theory of HTT in HD, where this gene drives early advantage followed by accelerated aging processes. 

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