Cornell scientists are investigating how human genetics influences gut microbiome functioning and raising awareness of the importance of human genetics in influencing the microbiome.
The
billions of bacteria that make up a person's gut microbiome have a significant
influence on metabolic function, illness, and general health. What's been less
obvious is how and to what degree the gut microbiota is formed by its human
host's genetics.
Finding the gene responsible for an illness or trait
that is produced by a single genetic mutation may be a pretty simple task.
However, a far more complicated process is when a group of genes combines to
cause illness or other phenotypic manifestation. There are many sequential
changes in the human genome from person to person and even between paired
chromosomes of the same person.
Single nucleotide polymorphism occurs when a
variation is caused by a single nucleotide substitution (SNP). Brito's team was
able to find SNPs that were linked to microbiome-related features, diseases,
and malignancies using a novel computational and modeling technique. In other
words, they were able to demonstrate that the human genome has direct impacts.
The current study was unique in that it made
advantage of this data format. It focused on the function of the gut microbiome
rather than the genetic makeup of each species in the agglomeration of
organisms that make up the microbiome; it looked at large groups of human genes
and their impact on microbiome functions rather than single genes, and it used
a novel strategy to model the distribution of functions and species within the
human gut.
Previous models did not suit the properties of
metagenomic sequencing data sets well. To account for these traits, Wells
proposed utilizing the Tweedie distribution, a sort of probability modeling.
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