Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number

Alexander N. Combes, Sean Wilson, Belinda Phipson, Brandon B. Binnie, Adler Ju, Kynan T. Lawlor, Cristina Cebrian, Sarah L. Walton, Ian M. Smyth, Karen M. Moritz, Raphael Kopan, Alicia Oshlack, Melissa H. Little

Research output: Contribution to journalArticleResearchpeer-review

Abstract

The regulation of final nephron number in the kidney is poorly understood. Cessation of nephron formation occurs when the self-renewing nephron progenitor population commits to differentiation. Transcription factors within this progenitor population, such as SIX2, are assumed to control expression of genes promoting self-renewal such that homozygous Six2 deletion results in premature commitment and an early halt to kidney development. In contrast, Six2 heterozygotes were assumed to be unaffected. Using quantitative morphometry, we found a paradoxical 18% increase in ureteric branching and final nephron number in Six2 heterozygotes, despite evidence for reduced levels of SIX2 protein and transcript. This was accompanied by a clear shift in nephron progenitor identity with a distinct subset of downregulated progenitor genes such as Cited1 and Meox1 while other genes were unaffected. The net result was an increase in nephron progenitor proliferation, as assessed by elevated EdU (5-ethynyl-2'-deoxyuridine) labeling, an increase in MYC protein, and transcriptional upregulation of MYC target genes. Heterozygosity for Six2 on an Fgf20-/- background resulted in premature differentiation of the progenitor population, confirming that progenitor regulation is compromised in Six2 heterozygotes. Overall, our studies reveal a unique dose response of nephron progenitors to the level of SIX2 protein in which the role of SIX2 in progenitor proliferation versus self-renewal is separable.

Original languageEnglish
Pages (from-to)589-598
Number of pages10
JournalKidney International
Volume93
Issue number3
DOIs
Publication statusPublished - Mar 2018

Keywords

  • Genetics
  • Imaging
  • Kidney development
  • Transcription regulation

Cite this

Combes, A. N., Wilson, S., Phipson, B., Binnie, B. B., Ju, A., Lawlor, K. T., ... Little, M. H. (2018). Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number. Kidney International, 93(3), 589-598. https://doi.org/10.1016/j.kint.2017.09.015
Combes, Alexander N. ; Wilson, Sean ; Phipson, Belinda ; Binnie, Brandon B. ; Ju, Adler ; Lawlor, Kynan T. ; Cebrian, Cristina ; Walton, Sarah L. ; Smyth, Ian M. ; Moritz, Karen M. ; Kopan, Raphael ; Oshlack, Alicia ; Little, Melissa H. / Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number. In: Kidney International. 2018 ; Vol. 93, No. 3. pp. 589-598.
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abstract = "The regulation of final nephron number in the kidney is poorly understood. Cessation of nephron formation occurs when the self-renewing nephron progenitor population commits to differentiation. Transcription factors within this progenitor population, such as SIX2, are assumed to control expression of genes promoting self-renewal such that homozygous Six2 deletion results in premature commitment and an early halt to kidney development. In contrast, Six2 heterozygotes were assumed to be unaffected. Using quantitative morphometry, we found a paradoxical 18{\%} increase in ureteric branching and final nephron number in Six2 heterozygotes, despite evidence for reduced levels of SIX2 protein and transcript. This was accompanied by a clear shift in nephron progenitor identity with a distinct subset of downregulated progenitor genes such as Cited1 and Meox1 while other genes were unaffected. The net result was an increase in nephron progenitor proliferation, as assessed by elevated EdU (5-ethynyl-2'-deoxyuridine) labeling, an increase in MYC protein, and transcriptional upregulation of MYC target genes. Heterozygosity for Six2 on an Fgf20-/- background resulted in premature differentiation of the progenitor population, confirming that progenitor regulation is compromised in Six2 heterozygotes. Overall, our studies reveal a unique dose response of nephron progenitors to the level of SIX2 protein in which the role of SIX2 in progenitor proliferation versus self-renewal is separable.",
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Combes, AN, Wilson, S, Phipson, B, Binnie, BB, Ju, A, Lawlor, KT, Cebrian, C, Walton, SL, Smyth, IM, Moritz, KM, Kopan, R, Oshlack, A & Little, MH 2018, 'Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number', Kidney International, vol. 93, no. 3, pp. 589-598. https://doi.org/10.1016/j.kint.2017.09.015

Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number. / Combes, Alexander N.; Wilson, Sean; Phipson, Belinda; Binnie, Brandon B.; Ju, Adler; Lawlor, Kynan T.; Cebrian, Cristina; Walton, Sarah L.; Smyth, Ian M.; Moritz, Karen M.; Kopan, Raphael; Oshlack, Alicia; Little, Melissa H.

In: Kidney International, Vol. 93, No. 3, 03.2018, p. 589-598.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number

AU - Combes, Alexander N.

AU - Wilson, Sean

AU - Phipson, Belinda

AU - Binnie, Brandon B.

AU - Ju, Adler

AU - Lawlor, Kynan T.

AU - Cebrian, Cristina

AU - Walton, Sarah L.

AU - Smyth, Ian M.

AU - Moritz, Karen M.

AU - Kopan, Raphael

AU - Oshlack, Alicia

AU - Little, Melissa H.

PY - 2018/3

Y1 - 2018/3

N2 - The regulation of final nephron number in the kidney is poorly understood. Cessation of nephron formation occurs when the self-renewing nephron progenitor population commits to differentiation. Transcription factors within this progenitor population, such as SIX2, are assumed to control expression of genes promoting self-renewal such that homozygous Six2 deletion results in premature commitment and an early halt to kidney development. In contrast, Six2 heterozygotes were assumed to be unaffected. Using quantitative morphometry, we found a paradoxical 18% increase in ureteric branching and final nephron number in Six2 heterozygotes, despite evidence for reduced levels of SIX2 protein and transcript. This was accompanied by a clear shift in nephron progenitor identity with a distinct subset of downregulated progenitor genes such as Cited1 and Meox1 while other genes were unaffected. The net result was an increase in nephron progenitor proliferation, as assessed by elevated EdU (5-ethynyl-2'-deoxyuridine) labeling, an increase in MYC protein, and transcriptional upregulation of MYC target genes. Heterozygosity for Six2 on an Fgf20-/- background resulted in premature differentiation of the progenitor population, confirming that progenitor regulation is compromised in Six2 heterozygotes. Overall, our studies reveal a unique dose response of nephron progenitors to the level of SIX2 protein in which the role of SIX2 in progenitor proliferation versus self-renewal is separable.

AB - The regulation of final nephron number in the kidney is poorly understood. Cessation of nephron formation occurs when the self-renewing nephron progenitor population commits to differentiation. Transcription factors within this progenitor population, such as SIX2, are assumed to control expression of genes promoting self-renewal such that homozygous Six2 deletion results in premature commitment and an early halt to kidney development. In contrast, Six2 heterozygotes were assumed to be unaffected. Using quantitative morphometry, we found a paradoxical 18% increase in ureteric branching and final nephron number in Six2 heterozygotes, despite evidence for reduced levels of SIX2 protein and transcript. This was accompanied by a clear shift in nephron progenitor identity with a distinct subset of downregulated progenitor genes such as Cited1 and Meox1 while other genes were unaffected. The net result was an increase in nephron progenitor proliferation, as assessed by elevated EdU (5-ethynyl-2'-deoxyuridine) labeling, an increase in MYC protein, and transcriptional upregulation of MYC target genes. Heterozygosity for Six2 on an Fgf20-/- background resulted in premature differentiation of the progenitor population, confirming that progenitor regulation is compromised in Six2 heterozygotes. Overall, our studies reveal a unique dose response of nephron progenitors to the level of SIX2 protein in which the role of SIX2 in progenitor proliferation versus self-renewal is separable.

KW - Genetics

KW - Imaging

KW - Kidney development

KW - Transcription regulation

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