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Status |
Public on Feb 27, 2024 |
Title |
Identification of expression patterns of FoxP1 in the kidneys using RiboTag mice and RNA sequencing |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing Other
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Summary |
Intercalated cells within renal tubules play a vital role in maintaining body acid-base balance through H+ and HCO3- secretion. Disruptions in intercalated cell differentiation or channel activity due to gene mutations can lead to distal renal tubular acidosis (dRTA), yet the precise mechanisms governing this process remain poorly understood. This study identified Foxp1 and its downstream factors as novel essential factors for intercalated cell differentiation, thus shed light on potential underlying mechanisms in some unresolved cases of dRTA.
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Overall design |
To investigate the role of Foxp1 in kidney collecting tube, we generated the Cdh16-cre;Foxp1fl/fl (thereafter denoted as FoxP1kspKO) by crossing the Foxp1fl/fl mice with the Cdh16-Cre (also known as the Ksp-Cre) mice. In these mice, FoxP1 is conditionally knocked out in kidney tubular cells and the absence Foxp1 expression in kidney tubular cells was confirmed by immunostaining.
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Contributor(s) |
Wu S, Lu D, Feng Y, Song R |
Citation(s) |
38332484 |
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Submission date |
Jul 26, 2023 |
Last update date |
Mar 06, 2024 |
Contact name |
RENHUA SONG |
E-mail(s) |
Renhua.song1989@gmail.com
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Phone |
61452667663
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Organization name |
Centenary Institute
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Lab |
Epigenetics and RNA Biology Program
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Street address |
Charles Perkins Centre - D17, Level 4 West. The University of Sydney Johns Hopkins Drive
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City |
Camperdown |
State/province |
NSW |
ZIP/Postal code |
2050 |
Country |
Australia |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE238268 |
Foxp1 is required for renal intercalated cell differentiation and acid-base regulation |
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Relations |
BioProject |
PRJNA998705 |