WNT3A

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Protein-coding gene in the species Homo sapiens

title: "WNT3A" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public description: "Protein-coding gene in the species Homo sapiens" topic_path: "uncategorized" source: "https://en.wikipedia.org/wiki/WNT3A" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

::summary Protein-coding gene in the species Homo sapiens ::

Protein Wnt-3a is a protein that in humans is encoded by the WNT3A gene.

The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have are critical in tissue homeostasis, embryonic development, and disease.

Signaling and Related Genes

WNT3A is highly related to the WNT3 gene in sequence and protein function. WNT3A and WNT3 signal similarly through primarily the beta-catenin/Tcf pathway. WNT3A is located in the genome beside the WNT9A gene across many vertebrates. Similarly, the WNT3 gene occurs in the genome beside the WNT9B gene. WNT9A and WNT9B signal through the beta-catenin/Tcf pathway but do not play related roles as WNT3A and WNT3 in the same cellular processes.

Role in Disease

WNT3A is not linked to particular genetic disorder in humans. Mice that have a genetic mutation in the WNT3A die during early embryogenesis and fail to correctly form axial tissues. Rodent Wnt3a promotes the beta-catenin/Tcf pathway which is tumor inducing and can cause cancer when expressed in particular cell populations.

Role in embryonic development

Embryonic development is the process where the body plan is created. From studies in vertebrate model systems we can infer the roles of particular genes in human anatomical structures. Wnt3a plays a role in these processes:

Body plan - [[Torso]]

Wnt3A patterns a multipotent stem cell population that form neurons, muscles, bones, and cartilage of the torso region. Wnt3a instructs these multipotent stems cells to form muscle, bone, and cartilage progenitors over forming neurons. Wnt3A also regulates the Notch pathway to control the segmentation clock needed for normal torso development

Left-Right patterning

Wnt3a is in a signaling pathway that activates the gene Nodal which is left side signaling determinant

Intestine - Colon

The colon portion of the gastrointestinal tract is completely dependent on Wnt3a and Wnt3a selectively causes the growth of colon progenitors

Neural crest

Wnt3a expands neural crest cells during early development

Blood cells

Wnt3a promotes hematopoietic stem cell self-renewal. Wnt3a is needed for myeloid but not B-lymphoid development at the progenitor level, and affected immature thymocyte differentiation

Brain - Hippocampus

Wnt3a is needed for formation of the hippocampus portion of the brain

Teeth

Wnt3a promotes stem cell properties of dental pulp stem cells

References

References

  1. "Entrez Gene: WNT3A wingless-type MMTV integration site family, member 3A".
  2. (March 1997). "Evidence that absence of Wnt-3a signaling promotes neuralization instead of paraxial mesoderm development in the mouse". Developmental Biology.
  3. (October 2019). "Role of Wnt3a in the pathogenesis of cancer, current status and prospective". Molecular Biology Reports.
  4. (May 2015). "Lineage tracing of neuromesodermal progenitors reveals novel Wnt-dependent roles in trunk progenitor cell maintenance and differentiation". Development.
  5. (March 2003). "Wnt3a plays a major role in the segmentation clock controlling somitogenesis". Developmental Cell.
  6. (December 2005). "Wnt3a links left-right determination with segmentation and anteroposterior axis elongation". Development.
  7. (December 2005). "Wnt3a links left-right determination with segmentation and anteroposterior axis elongation". Development.
  8. (April 2020). "A dorsal-ventral gradient of Wnt3a/β-catenin signals controls mouse hindgut extension and colon formation". Development.
  9. (October 1997). "Wnt signalling required for expansion of neural crest and CNS progenitors". Nature.
  10. (January 2009). "Wnt3a deficiency irreversibly impairs hematopoietic stem cell self-renewal and leads to defects in progenitor cell differentiation". Blood.
  11. (February 2000). "A local Wnt-3a signal is required for development of the mammalian hippocampus". Development.
  12. (March 2020). "Wnt-3a Induces Epigenetic Remodeling in Human Dental Pulp Stem Cells". Cells.

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