University of Illinois at Chicago
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Wnt/β-catenin Pathway Functions by Inactivation of Tcf7l1 Protein

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posted on 2014-06-20, 00:00 authored by Chun-I Wu
The canonical Wnt/β-catenin signaling pathway classically functions through the activation of target genes by Tcf/Lef–β-catenin complexes. Each Tcf/Lef in mammals is believed to function as a switch, going from a transcriptional repressor in the absence of Wnt stabilized β-catenin to a transcriptional activator in the presence of Wnt-stabilized β-catenin. I determined that mouse Tcf7l1 (formerly named Tcf3) mediates a distinct and new form of regulation of the pathway, which is independent of transactivator activity of Tcf7l1-β-catenin complexes. Instead of switching Tcf7l1 into a transactivator, Wnt/β-catenin reduces Tcf7l1 protein levels, which relieves repression of target genes, such as Lef1. Experiments using mouse embryonic stem cells show that recombinant Wnt3a, GSK3-inhibition, or simply increasing β-catenin levels were all sufficient to reduce Tcf7l1 protein independent of mRNA levels. The effect did not occur in Tcf7l1ΔN/ΔN ES cells, which lack nine Tcf7l1 residues necessary for binding to β-catenin. Thus, β-catenin binding to Tcf7l1 is necessary and sufficient for destabilizing Tcf7l1 protein in stem cells. We ablated the Tcf7l1-β-catenin interaction by generating a mouse Tcf7l1ΔN knockin allele and show Tcf7l1ΔN blocks Wnt-reduction of Tcf7l1, inhibits Lef1 expression, and causes peri-natal lethality in Tcf7l1ΔN/ΔN mice. Interestingly, Tcf7l1-/ΔN mice developed into viable and ostensibly normal adult mice, demonstrating that reducing the amount of Tcf7l1 replaced the requirement for Tcf7l1-β-catenin interaction. These findings impact understanding of the mechanisms whereby Wnt/β-catenin mediates its effects, especially in Tcf7l1-expressing stem cells and tumor cells.

History

Advisor

Merrill, Bradley

Department

Biochemistry and Molecular Genetics

Degree Grantor

University of Illinois at Chicago

Degree Level

  • Doctoral

Committee Member

Benevolenskaya, Elizaveta Frolov, Maxim Lau, Lester Schmidt, Jennifer

Submitted date

2014-05

Language

  • en

Issue date

2014-06-20

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