TY - JOUR
T1 - Truncated SALL1 Impedes Primary Cilia Function in Townes-Brocks Syndrome
AU - Bozal-Basterra, Laura
AU - Martín-Ruíz, Itziar
AU - Pirone, Lucia
AU - Liang, Yinwen
AU - Sigurdsson, Jón Otti
AU - Gonzalez-Santamarta, Maria
AU - Giordano, Immacolata
AU - Gabicagogeascoa, Estibaliz
AU - de Luca, Angela
AU - Rodríguez, Jose A.
AU - Wilkie, Andrew O.M.
AU - Kohlhase, Jürgen
AU - Eastwood, Deborah
AU - Yale, Christopher
AU - Olsen, Jesper V.
AU - Rauchman, Michael
AU - Anderson, Kathryn V.
AU - Sutherland, James D.
AU - Barrio, Rosa
N1 - Publisher Copyright:
© 2017 The Author(s)
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Townes-Brocks syndrome (TBS) is characterized by a spectrum of malformations in the digits, ears, and kidneys. These anomalies overlap those seen in a growing number of ciliopathies, which are genetic syndromes linked to defects in the formation or function of the primary cilia. TBS is caused by mutations in the gene encoding the transcriptional repressor SALL1 and is associated with the presence of a truncated protein that localizes to the cytoplasm. Here, we provide evidence that SALL1 mutations might cause TBS by means beyond its transcriptional capacity. By using proximity proteomics, we show that truncated SALL1 interacts with factors related to cilia function, including the negative regulators of ciliogenesis CCP110 and CEP97. This most likely contributes to more frequent cilia formation in TBS-derived fibroblasts, as well as in a CRISPR/Cas9-generated model cell line and in TBS-modeled mouse embryonic fibroblasts, than in wild-type controls. Furthermore, TBS-like cells show changes in cilia length and disassembly rates in combination with aberrant SHH signaling transduction. These findings support the hypothesis that aberrations in primary cilia and SHH signaling are contributing factors in TBS phenotypes, representing a paradigm shift in understanding TBS etiology. These results open possibilities for the treatment of TBS.
AB - Townes-Brocks syndrome (TBS) is characterized by a spectrum of malformations in the digits, ears, and kidneys. These anomalies overlap those seen in a growing number of ciliopathies, which are genetic syndromes linked to defects in the formation or function of the primary cilia. TBS is caused by mutations in the gene encoding the transcriptional repressor SALL1 and is associated with the presence of a truncated protein that localizes to the cytoplasm. Here, we provide evidence that SALL1 mutations might cause TBS by means beyond its transcriptional capacity. By using proximity proteomics, we show that truncated SALL1 interacts with factors related to cilia function, including the negative regulators of ciliogenesis CCP110 and CEP97. This most likely contributes to more frequent cilia formation in TBS-derived fibroblasts, as well as in a CRISPR/Cas9-generated model cell line and in TBS-modeled mouse embryonic fibroblasts, than in wild-type controls. Furthermore, TBS-like cells show changes in cilia length and disassembly rates in combination with aberrant SHH signaling transduction. These findings support the hypothesis that aberrations in primary cilia and SHH signaling are contributing factors in TBS phenotypes, representing a paradigm shift in understanding TBS etiology. These results open possibilities for the treatment of TBS.
KW - BioID
KW - SALL1
KW - Townes-Brocks syndrome
KW - primary cilia
KW - rare disease
KW - spalt
UR - https://www.scopus.com/pages/publications/85045398895
U2 - 10.1016/j.ajhg.2017.12.017
DO - 10.1016/j.ajhg.2017.12.017
M3 - Article
C2 - 29395072
AN - SCOPUS:85045398895
SN - 0002-9297
VL - 102
SP - 249
EP - 265
JO - American journal of human genetics
JF - American journal of human genetics
IS - 2
ER -