Siah-1 mediates a novel beta-catenin degradation pathway linking p53 to the adenomatous polyposis coli protein (Q24291288)

protein catabolic process

GOA release 2020-03-11

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GOA release 2020-03-11

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J Liu

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J Stevens

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C A Rote

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H J Yost

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Y Hu

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K L Neufeld

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R L White

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N Matsunami

Isolation of 10 differentially expressed cDNAs in p53-induced apoptosis: activation of the vertebrate homologue of the drosophila seven in absentia gene

8

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publication date

May 2001

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language of work or name

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7

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issue

5

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page(s)

927-36

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SIAH-1 inhibits cell growth by altering the mitotic process

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The ubiquitin-proteasome pathway and serine kinase activity modulate adenomatous polyposis coli protein-mediated regulation of beta-catenin-lymphocyte enhancer-binding factor signaling

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A targeted chain-termination mutation in the mouse Apc gene results in multiple intestinal tumors

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The F-box protein beta-TrCP associates with phosphorylated beta-catenin and regulates its activity in the cell.

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Siah-1 N-terminal RING domain is required for proteolysis function, and C-terminal sequences regulate oligomerization and binding to target proteins

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Characterization of Human Homologs of theDrosophila seven in absentia(sina) Gene

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Mammalian homologs of seven in absentia regulate DCC via the ubiquitin–proteasome pathway

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The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos

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An F-box protein, FWD1, mediates ubiquitin-dependent proteolysis of beta-catenin

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Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC-/- colon carcinoma

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Photoreceptor Cell Differentiation Requires Regulated Proteolysis of the Transcriptional Repressor Tramtrack

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p21 WAF-1 reorganizes the nucleus in tumor suppression

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Siah-1, SIP, and Ebi collaborate in a novel pathway for beta-catenin degradation linked to p53 responses

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p53-inducible human homologue of Drosophila seven in absentia (Siah) inhibits cell growth: suppression by BAG-1

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Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC

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Regulation of intracellular beta-catenin levels by the adenomatous polyposis coli (APC) tumor-suppressor protein

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Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppression

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APC-mediated downregulation of beta-catenin activity involves nuclear sequestration and nuclear export

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Exogenous expression of beta-catenin regulates contact inhibition, anchorage-independent growth, anoikis, and radiation-induced cell cycle arrest

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Loss of Apc heterozygosity and abnormal tissue building in nascent intestinal polyps in mice carrying a truncated Apc gene

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Wnt signaling in oncogenesis and embryogenesis--a look outside the nucleus

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APC mutations occur early during colorectal tumorigenesis

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SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1)

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Cytoskeletal reorganization by soluble Wnt-3a protein signalling

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The APC gene product in normal and tumor cells

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Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center

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Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development

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Multiple intestinal neoplasia caused by a mutation in the murine homolog of the APC gene

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PHYL acts to down-regulate TTK88, a transcriptional repressor of neuronal cell fates, by a SINA-dependent mechanism.

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p53 suppresses the c-Myb-induced activation of heat shock transcription factor 3.

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Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli

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Tumor Suppressing Pathways

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The SCFbeta-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IkappaBalpha and beta-catenin and stimulates IkappaBalpha ubiquitination in vitro

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Proteasomal regulation of nuclear receptor corepressor-mediated repression

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11389840

1 reference

Consolidated OpenCitations Corpus – April 2017