Glycosylation modification is an important post-translational modification of proteins. According to the different ways of linking the sugar chain and protein, glycosylation modification is mainly divided into two types: N-glycosylation and O-glycosylation. One of the most common O-glycosylation modifications is mucin-type O-glycosylation. With continuous research, more and more tumor markers are being discovered. These include several members of the GALNT family, which is the initiating enzyme that catalyzes mucin-type O-glycosylation. It affects the O-glycosylation of mucins, thereby influencing tumor cell genesis, prognosis, proliferation, and migration. To date, 20 isoforms of GALNT have been identified in humans. There are lots of research reports on GALNT related to cancer and other diseases.
CD BioGlyco is committed to being a reliable GALNT gene modification service partner. We have rich experience in cell lines and animal model construction.
Fig.1 One-stop GALNT gene modification process. (CD BioGlyco)
GALNT2
GALNT2 modifies the O-glycosylation of ITGA5. It affects the activation of PI3K/Akt and MAPK/ERK pathways. Studies have shown that the knockdown of GALNT2 inhibits cell proliferation, migration, and invasion of non-small cell lung carcinoma cells. While the overexpression of GALNT2 resulted in the opposite.
GALNT3
GALNT3 affects the differentiation and prognosis of colon cancer cells. It may be a reliable diagnostic indicator for colon cancer. GALNT3 also affects the LDN-glycosylation of sclerostin, which may open up a new tool for the treatment of bone-specific osteoporosis.
GALNT6
GALNT6 is used as a molecular diagnostic marker for mammary carcinoma cell proliferation. Knockdown of GALNT6 inhibits cell migration and invasion of hepatocellular carcinoma (HCC) cells.
GALNT13
GALNT13 is highly correlated with the development and prognosis of myeloid neuroblastoma. It is used as a molecular marker for the diagnosis of myeloid neuroblastoma.
GALNT14
Mucin-type O-glycosylation in cancer varies in structure and amount, culminating in a unique glycan structure. GALNT14 plays an important role in a wide range of biological activities, including tumorigenesis, progression, invasion, migration, and apoptosis.
Paper Title: B4GALNT3 regulates glycosylation of sclerostin and bone mass
Technology: Gene Knockout, Gene Overexpression, Gene Silencing
Journal: EBioMedicine
IF: 11.1
Published: 2023
Results: B4GALNT3 expresses β-1,4-N-acetylgalactosaminyltransferase 3. Serum total sclerostin levels were elevated but serum LDN-glycosylated sclerostin levels were decreased in B4GALNT3 knockout mice compared to controls. The silencing of B4GALNT3 decreased the levels of LDN-glycosylated sclerostin, whereas overexpression of B4GALNT3 decreased the levels. B4GALNT3-mediated LDN-glycosylation of sclerostin may be a target for bone-specific osteoporosis.
Fig. 2 Changes in sclerostin levels in B4galnt3 knockout mice. (Movérare-Skrtic, et al., 2023)
CD BioGlyco has undergone continuous research to minimize the time required to prepare gene-edited cells and animal models. We use optimized technologies for gene editing to precisely modify genes. If you are interested in our GALNT gene modification service, please feel free to contact us.
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