Back

Constitutive Yap activation in distal nephron segments disrupts epithelial identity and nephron patterning

Dehghani-Ghobadi, Z.; Chung, E.; Sayed, M.; Ahn, C.; Hu, Y.-C.; Lim, H.-W.; Park, J.-S.

2025-12-13 developmental biology
10.64898/2025.12.10.693519 bioRxiv
Show abstract

BackgroundThe distal convoluted tubule (DCT) and connecting tubule (CNT) are critical for fine-tuning electrolyte reabsorption and maintaining renal homeostasis. While the Hippo pathway effector Yap is known to regulate kidney development, its specific role within the distal nephron segments remains unknown. MethodsTo investigate Yap function in the distal nephron segments, we generated a Cre-inducible Yap gain-of-function allele (Col1a1-Yap5SA) and a distal nephron-specific Slc12a3Cre to drive an active form of Yap in the distal nephron segments. We performed phenotypic assessments along with molecular and transcriptomic analyses to examine changes in epithelial organization and nephron segmentation. ResultsLineage tracing showed that Slc12a3Cre targets both DCT and CNT, suggesting that CNT cells arise from Slc12a3+ DCT cells. Constitutive Yap activation in these segments caused increased proliferation and ectopic cell migration into adjacent nephron segments. This was accompanied by disrupted expression of DCT/CNT marker genes, loss of apicobasal polarity, and compromised junctional architecture, indicating epithelial-to-mesenchymal transition. Notably, mutant kidneys also exhibited downregulation of proximal tubule markers, indicating a non-cell-autonomous effect. ConclusionsOur findings demonstrate that sustained Yap activation in the distal nephron segments disrupts epithelial identity and structure while also exerting non-cell-autonomous effects on nephron patterning, particularly in the proximal tubule. These results underscore the importance of tightly regulated Hippo-Yap signaling in maintaining epithelial integrity and proper nephron segmentation. Key PointsO_LIA novel Slc12a3Cre targets both distal and connecting tubules in the mouse kidney, revealing the developmental origin of connecting tubules. C_LIO_LIConstitutive Yap activation in distal nephron segments disrupts their segmental identity, leading to epithelial-to-mesenchymal transition. C_LIO_LIConstitutive Yap activation in distal nephron segments suppresses expression of proximal tubule-specific genes. C_LI

Matching journals

The top 3 journals account for 50% of the predicted probability mass.

1
PLOS ONE
4510 papers in training set
Top 8%
19.0%
2
American Journal of Physiology-Renal Physiology
25 papers in training set
Top 0.1%
17.9%
3
Journal of the American Society of Nephrology
52 papers in training set
Top 0.1%
15.0%
50% of probability mass above
4
Kidney360
22 papers in training set
Top 0.1%
8.4%
5
Developmental Biology
134 papers in training set
Top 0.5%
6.5%
6
Scientific Reports
3102 papers in training set
Top 28%
4.3%
7
JCI Insight
241 papers in training set
Top 2%
2.1%
8
Frontiers in Physiology
93 papers in training set
Top 2%
2.1%
9
Journal of Cellular and Molecular Medicine
18 papers in training set
Top 0.5%
1.3%
10
Developmental Dynamics
50 papers in training set
Top 0.6%
0.9%
11
The FASEB Journal
175 papers in training set
Top 2%
0.9%
12
Frontiers in Cell and Developmental Biology
218 papers in training set
Top 7%
0.9%
13
Nature Communications
4913 papers in training set
Top 60%
0.8%
14
Biology Open
130 papers in training set
Top 3%
0.8%
15
Human Mutation
29 papers in training set
Top 0.7%
0.8%
16
iScience
1063 papers in training set
Top 31%
0.8%
17
Kidney International Reports
14 papers in training set
Top 0.3%
0.8%
18
Differentiation
11 papers in training set
Top 0.3%
0.7%
19
Cytometry Part A
30 papers in training set
Top 0.3%
0.7%
20
The Journal of Pharmacology and Experimental Therapeutics
15 papers in training set
Top 0.5%
0.7%
21
Diabetologia
36 papers in training set
Top 1%
0.7%
22
PLOS Genetics
756 papers in training set
Top 17%
0.7%
23
Cardiovascular Research
33 papers in training set
Top 1%
0.7%
24
eneuro
389 papers in training set
Top 11%
0.5%