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The molecular pathways that regulate the transition from renal progenitor to renal vesicle are not well understood. Here we show that Sall1interacts with the Nucleosome Remodeling and Deacetylase Complex (NuRD) to inhibit premature differentiation of nephron progenitor cells. Disruption of Sall1-NuRD in vivo in knock-in mice (\u0394SRM) resulted in accelerated differentiation of nephron progenitors and bilateral renal hypoplasia. Transcriptional profiling of mutant kidneys revealed a striking pattern in which genes of the glomerular and proximal tubule lineages were either unchanged or upregulated, and those in the loop of Henle and distal tubule lineages were downregulated. These global changes in gene expression were accompanied by a significant decrease in THP, NKCC2, AQP-1 positive loop of Henle nephron segments in mutant \u0394SRM kidneys. These findings highlight an important function of Sall1-NuRD interaction in the regulation of Six2 positive multipotent renal progenitor cells and formation of the loop of Henle.<\/jats:p>","DOI":"10.1242\/dev.148692","type":"journal-article","created":{"date-parts":[[2017,8,1]],"date-time":"2017-08-01T00:30:21Z","timestamp":1501547421000},"source":"Crossref","is-referenced-by-count":13,"title":["Sall1-NuRD interaction regulates multipotent nephron progenitors and is required for loop of Henle formation"],"prefix":"10.1242","author":[{"given":"Jeannine M.","family":"Basta","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, Saint Louis University, St. Louis MO 63104, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lynn","family":"Robbins","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Saint Louis University, St. Louis MO 63104, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Darcy R.","family":"Denner","sequence":"additional","affiliation":[{"name":"Department of Biochemistry and Molecular Biology, Saint Louis University, St. Louis MO 63104, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Grant R.","family":"Kolar","sequence":"additional","affiliation":[{"name":"Department of Pathology, Saint Louis University, St. Louis MO 63104, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4820-3689","authenticated-orcid":false,"given":"Michael","family":"Rauchman","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Saint Louis University, St. Louis MO 63104, USA"},{"name":"Department of Biochemistry and Molecular Biology, Saint Louis University, St. Louis MO 63104, USA"},{"name":"VA St. Louis Health Care System, John Cochran Division, St. Louis, MO 63106, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2017,1,1]]},"reference":[{"key":"2021042608532036800_DEV148692C1","doi-asserted-by":"publisher","first-page":"1191","DOI":"10.1016\/j.devcel.2012.04.018","article-title":"FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man","volume":"22","author":"Barak","year":"2012","journal-title":"Dev. 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