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How Fucose of Blood Group Glycotopes Programs Human Gut Microbiota
1Institute of Protein Research, Russian Academy of Sciences, Pushchino, Moscow Region, 142290, Russia. skonon23@gmail.com.
Biochemistry. Biokhimiia
|October 10, 2017
Summary
Gut microbiota development in infants is crucial for health. Genes FUT2 and FUT3 control the selection of beneficial gut microbes using fucosylated structures in breast milk and mucins.
Area of Science:
- Microbiology
- Human Physiology
- Genetics
Background:
- Gut microbiota formation is vital for infant health, particularly during the first two years of life.
- The development of a healthy gut microbiome is influenced by genetic factors and early-life nutrition.
- FUT2 and FUT3 genes play a key role in synthesizing specific glycan structures essential for microbial interactions.
Purpose of the Study:
- To review the mechanisms by which fucosylated oligosaccharides in breast milk and mucins influence gut microbiota selection and maintenance in newborns.
- To explore the reasons behind fucose's role as a primary selection signal over sialic acid in early gut microbial colonization.
Main Methods:
- Literature review focusing on the roles of FUT2 and FUT3 genes.
- Analysis of the biochemical pathways involved in fucosylation.
- Examination of the interaction between host glycan structures and microbial communities.
Main Results:
- FUT2 and FUT3 genes encode fucosyltransferases, crucial for creating fucosylated glycans.
- These glycans act as binding sites or signals for specific mutualistic microorganisms.
- Fucose serves as a key biological signal for selecting and maintaining beneficial gut bacteria.
Conclusions:
- Fucosylated structures derived from breast milk and intestinal mucins are critical mediators in establishing a healthy infant gut microbiota.
- The genetic control of fucosylation by FUT2 and FUT3 highlights a targeted mechanism for beneficial microbial colonization.
- Understanding these mechanisms provides insights into promoting infant gut health through nutritional and genetic interactions.
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