Literature DB >> 21292980

The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.

Derek E Gildea1, Erin S Luetkemeier, Xiaozhong Bao, Stacie K Loftus, Susan Mackem, Yingzi Yang, William J Pavan, Leslie G Biesecker.   

Abstract

Polydactyly is a common malformation and can be an isolated anomaly or part of a pleiotropic syndrome. The elucidation of the mutated genes that cause polydactyly provides insight into limb development pathways. The extra-toes spotting (Xs) mouse phenotype manifests anterior polydactyly, predominantly in the forelimbs, with ventral hypopigmenation. The mapping of Xs(J) to chromosome 7 was confirmed, and the interval was narrowed to 322 kb using intersubspecific crosses. Two mutations were identified in eukaryotic translation initiation factor 3 subunit C (Eif3c). An Eif3c c.907C>T mutation (p.Arg303X) was identified in Xs(J), and a c.1702_1758del mutation (p.Leu568_Leu586del) was identified in extra-toes spotting-like (Xsl), an allele of Xs(J). The effect of the Xs(J) mutation on the SHH/GLI3 pathway was analyzed by in situ hybridization analysis, and we show that Xs mouse embryos have ectopic Shh and Ptch1 expression in the anterior limb. In addition, anterior limb buds show aberrant Gli3 processing, consistent with perturbed SHH/GLI3 signaling. Based on the occurrence of Eif3c mutations in 2 Xs lines and haploinsufficiency of the Xs(J) allele, we conclude that the Xs phenotype is caused by a mutation in Eif3c, a component of the translation initiation complex, and that the phenotype is associated with aberrant SHH/GLI3 signaling.

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Year:  2011        PMID: 21292980      PMCID: PMC3079303          DOI: 10.1096/fj.10-169771

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  33 in total

Review 1.  Hedgehog signaling in animal development: paradigms and principles.

Authors:  P W Ingham; A P McMahon
Journal:  Genes Dev       Date:  2001-12-01       Impact factor: 11.361

2.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

Authors:  K J Livak; T D Schmittgen
Journal:  Methods       Date:  2001-12       Impact factor: 3.608

3.  The yeast eIF3 subunits TIF32/a, NIP1/c, and eIF5 make critical connections with the 40S ribosome in vivo.

Authors:  Leos Valásek; Amy A Mathew; Byung-Sik Shin; Klaus H Nielsen; Béla Szamecz; Alan G Hinnebusch
Journal:  Genes Dev       Date:  2003-03-15       Impact factor: 11.361

4.  Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning.

Authors:  Mustafa K Khokha; David Hsu; Lisa J Brunet; Marc S Dionne; Richard M Harland
Journal:  Nat Genet       Date:  2003-07       Impact factor: 38.330

Review 5.  The molecular foundations of the maternal to zygotic transition in the preimplantation embryo.

Authors:  Richard M Schultz
Journal:  Hum Reprod Update       Date:  2002 Jul-Aug       Impact factor: 15.610

6.  Direct eIF2-eIF3 contact in the multifactor complex is important for translation initiation in vivo.

Authors:  Leos Valásek; Klaus H Nielsen; Alan G Hinnebusch
Journal:  EMBO J       Date:  2002-11-01       Impact factor: 11.598

7.  Mutation of melanosome protein RAB38 in chocolate mice.

Authors:  Stacie K Loftus; Denise M Larson; Laura L Baxter; Anthony Antonellis; Yidong Chen; Xufeng Wu; Yuan Jiang; Michael Bittner; John A Hammer; William J Pavan
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-26       Impact factor: 11.205

8.  Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud.

Authors:  Kazushi Aoto; Tamiko Nishimura; Kazuhiro Eto; Jun Motoyama
Journal:  Dev Biol       Date:  2002-11-15       Impact factor: 3.582

9.  Twist plays an essential role in FGF and SHH signal transduction during mouse limb development.

Authors:  Meredith P O'Rourke; Kenneth Soo; Richard R Behringer; Chi-Chung Hui; Patrick P L Tam
Journal:  Dev Biol       Date:  2002-08-01       Impact factor: 3.582

10.  The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival.

Authors:  Martina Barkić; Sladana Crnomarković; Kristina Grabusić; Ivana Bogetić; Linda Panić; Sanda Tamarut; Maja Cokarić; Ines Jerić; Sandra Vidak; Sinisa Volarević
Journal:  Mol Cell Biol       Date:  2009-03-09       Impact factor: 4.272

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  4 in total

1.  Controlling tissue patterning by translational regulation of signaling transcripts through the core translation factor eIF3c.

Authors:  Kotaro Fujii; Olena Zhulyn; Gun Woo Byeon; Naomi R Genuth; Craig H Kerr; Erin M Walsh; Maria Barna
Journal:  Dev Cell       Date:  2021-11-08       Impact factor: 12.270

2.  Human eIF3b and eIF3a serve as the nucleation core for the assembly of eIF3 into two interconnected modules: the yeast-like core and the octamer.

Authors:  Susan Wagner; Anna Herrmannová; Darina Šikrová; Leoš Shivaya Valášek
Journal:  Nucleic Acids Res       Date:  2016-10-19       Impact factor: 16.971

3.  Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model.

Authors:  Richard L Mort; Robert J H Ross; Kirsten J Hainey; Olivia J Harrison; Margaret A Keighren; Gabriel Landini; Ruth E Baker; Kevin J Painter; Ian J Jackson; Christian A Yates
Journal:  Nat Commun       Date:  2016-01-06       Impact factor: 14.919

4.  Eukaryotic translation initiation factor 3 (eIF3) subunit e is essential for embryonic development and cell proliferation.

Authors:  Daichi Sadato; Tomio Ono; Saki Gotoh-Saito; Naoki Kajiwara; Namiko Nomura; Masako Ukaji; Liying Yang; Kenji Sakimura; Youichi Tajima; Keisuke Oboki; Futoshi Shibasaki
Journal:  FEBS Open Bio       Date:  2018-07-05       Impact factor: 2.693

  4 in total

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