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Canonical Wnt Signaling Pathway02:54

Canonical Wnt Signaling Pathway

The gene encoding the main signaling molecules of the Wnt signaling pathways (the Wnt proteins) was discovered almost four decades ago by Nüsslein-Volhard and Wieschaus. They identified and originally named the gene "wingless" (wg) after a phenotype discovered during their landmark genetic screen in Drosophila for body pattern defects. At around the same time, another researcher named Harold Varmus found that a murine tumor virus activates the mammalian wg homolog, Int-1, which results in tumor...
Canonical Wnt Signaling Pathway02:54

Canonical Wnt Signaling Pathway

The gene encoding the main signaling molecules of the Wnt signaling pathways (the Wnt proteins) was discovered almost four decades ago by Nüsslein-Volhard and Wieschaus. They identified and originally named the gene "wingless" (wg) after a phenotype discovered during their landmark genetic screen in Drosophila for body pattern defects. At around the same time, another researcher named Harold Varmus found that a murine tumor virus activates the mammalian wg homolog, Int-1, which results in tumor...
Non-Canonical Wnt Signaling Pathways01:41

Non-Canonical Wnt Signaling Pathways

Wnt is a zygotic effect gene that is expressed during very early embryonic development. It regulates various processes in animals starting from early development through the adult stage, such as organogenesis in the embryo and maintenance of neuronal and blood stem cells. Wnt proteins can induce a wide variety of intracellular pathways depending upon the specific abilities of different Wnt ligands to form a complex with shared and cognate receptors in the presence of different co-receptors. The...
Non-Canonical Wnt Signaling Pathways01:41

Non-Canonical Wnt Signaling Pathways

Wnt is a zygotic effect gene that is expressed during very early embryonic development. It regulates various processes in animals starting from early development through the adult stage, such as organogenesis in the embryo and maintenance of neuronal and blood stem cells. Wnt proteins can induce a wide variety of intracellular pathways depending upon the specific abilities of different Wnt ligands to form a complex with shared and cognate receptors in the presence of different co-receptors. The...
Development of the Sexual Organs in the Embryo and Fetus01:15

Development of the Sexual Organs in the Embryo and Fetus

Development of the reproductive organs in an embryo starts from a bipotential state. This means the early embryo can develop either male or female reproductive organs. The formation of these organs begins with the growth of gonadal ridges that arise from the intermediate mesoderm during the fifth week of development.
Near the gonadal ridges, two duct systems are present: the mesonephric ducts (Wolffian ducts) and paramesonephric ducts (Müllerian ducts). These ducts form the basis for the male...
Catenins01:23

Catenins

Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the adherens...

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Related Experiment Video

Updated: Jun 28, 2026

Modeling Paracrine Noncanonical Wnt Signaling In Vitro
11:14

Modeling Paracrine Noncanonical Wnt Signaling In Vitro

Published on: December 10, 2021

WNT4 and sex development.

A Biason-Lauber1, D Konrad

  • 1University Children's Hospital, Zurich, Switzerland. Anna.Lauber@kispi.uzh.ch

Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation
|November 7, 2008
PubMed
Summary
This summary is machine-generated.

The WNT4 gene is crucial for female sexual development, directing gonad development towards ovaries. WNT4 gene defects cause uterine absence and androgen excess, distinguishing it from typical Mayer-Rokitansky-Kuster-Hauser syndrome.

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Studying Wnt Signaling During Patterning of Conducting Airways
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Studying Wnt Signaling During Patterning of Conducting Airways

Published on: October 16, 2016

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Last Updated: Jun 28, 2026

Modeling Paracrine Noncanonical Wnt Signaling In Vitro
11:14

Modeling Paracrine Noncanonical Wnt Signaling In Vitro

Published on: December 10, 2021

Studying Wnt Signaling During Patterning of Conducting Airways
13:00

Studying Wnt Signaling During Patterning of Conducting Airways

Published on: October 16, 2016

Area of Science:

  • Genetics
  • Developmental Biology
  • Endocrinology

Background:

  • Male sexual differentiation pathways are well-understood, but female pathways remain less defined.
  • No specific genes were previously identified for ovarian development analogous to SRY/SOX9 in testicular development.
  • WNT4 is known to regulate female reproductive tract development, antagonize testosterone, and support oocyte development in mice.

Purpose of the Study:

  • To elucidate the role of WNT4 in female sexual differentiation and gonad development.
  • To identify WNT4 as a key gene directing bipotential gonads towards ovarian development in humans.
  • To establish WNT4 deficiency as a distinct clinical entity based on specific symptoms.

Main Methods:

  • Review of existing literature on sexual differentiation genes.
  • Analysis of clinical data from patients with WNT4 defects.
  • Comparison of WNT4 deficiency symptoms with Mayer-Rokitansky-Kuster-Hauser syndrome.

Main Results:

  • WNT4 is the first identified human gene to direct bipotential gonad development towards ovaries.
  • Heterozygous WNT4 defects in patients are associated with Mullerian agenesis and ovarian hyperandrogenism.
  • Absence of the uterus and androgen excess are pathognomonic signs of WNT4 defects.

Conclusions:

  • WNT4 plays a critical role in human ovarian development.
  • WNT4 deficiency presents a distinct clinical picture characterized by uterine absence and androgen excess.
  • WNT4 deficiency may represent a separate clinical entity from Mayer-Rokitansky-Kuster-Hauser syndrome.