<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Karner CM</submitter><funding>NIDDK NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>2014-23</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2925040</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>239(7)</volume><pubmed_abstract>Recent studies using small molecule antagonists have revealed that the poly(ADP-ribose) polymerases (PARPs) Tankyrase 1 and 2 are critical regulators of canonical Wnt signaling in some cellular contexts. However, the absence of any activity during zebrafish embryogenesis suggested that the tankyrases may not be general/core components of the Wnt pathway. Here, we show that Tnks1 and 2 are broadly expressed during mouse development and are essential during kidney and lung development. In the kidney, blockage of tankyrase activity phenocopies the effect of blocking production of all Wnt ligands. Tankyrase inhibition can be rescued by activation of beta-catenin demonstrating its specificity for the Wnt pathway. In addition, treatment with tankyrase inhibitors appears to be completely reversib</pubmed_abstract><journal>Developmental dynamics : an official publication of the American Association of Anatomists</journal><pubmed_title>Tankyrase is necessary for canonical Wnt signaling during kidney development.</pubmed_title><pmcid>PMC2925040</pmcid><funding_grant_id>R01DK080004</funding_grant_id><funding_grant_id>R01GM079554</funding_grant_id><funding_grant_id>R01 GM076398</funding_grant_id><funding_grant_id>R01 GM079554</funding_grant_id><funding_grant_id>R01GM076398</funding_grant_id><funding_grant_id>R01 DK080004</funding_grant_id><pubmed_authors>Merkel CE</pubmed_authors><pubmed_authors>Lum L</pubmed_authors><pubmed_authors>Carroll TJ</pubmed_authors><pubmed_authors>Karner CM</pubmed_authors><pubmed_authors>Dodge M</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Ma Z</pubmed_authors><pubmed_authors>Chen C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tankyrase is necessary for canonical Wnt signaling during kidney development.</name><description>Recent studies using small molecule antagonists have revealed that the poly(ADP-ribose) polymerases (PARPs) Tankyrase 1 and 2 are critical regulators of canonical Wnt signaling in some cellular contexts. However, the absence of any activity during zebrafish embryogenesis suggested that the tankyrases may not be general/core components of the Wnt pathway. Here, we show that Tnks1 and 2 are broadly expressed during mouse development and are essential during kidney and lung development. In the kidney, blockage of tankyrase activity phenocopies the effect of blocking production of all Wnt ligands. Tankyrase inhibition can be rescued by activation of beta-catenin demonstrating its specificity for the Wnt pathway. In addition, treatment with tankyrase inhibitors appears to be completely reversib</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jul</publication><modification>2026-04-07T17:39:04.091Z</modification><creation>2019-03-27T00:33:27Z</creation></dates><accession>S-EPMC2925040</accession><cross_references><pubmed>20549720</pubmed><doi>10.1002/dvdy.22340</doi></cross_references></HashMap>