Literature DB >> 8026341

msd is required for mesoderm induction in mice.

B C Holdener1, C Faust, N S Rosenthal, T Magnuson.   

Abstract

Mesoderm induction is fundamental for establishing the basic body plan of the vertebrate embryo and mutations are critical for dissecting this process. Mouse embryos lacking msd (mesoderm deficiency) do not produce mesoderm but have well-defined extraembryonic and thickened embryonic ectoderm. Distribution of transcripts indicate that temporal regulation of gene expression relevant to gastrulation has begun but primitive-streak formation and mesoderm induction are blocked. Both msd-deficient embryos and embryonic stem (ES) cells fail to form highly differentiated structures of mesoderm origin, but are capable of ectodermal differentiation. Thus, the effects of the msd mutation are restricted to mesoderm formation and could result from the inability to respond to an inducing signal.

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Year:  1994        PMID: 8026341     DOI: 10.1242/dev.120.5.1335

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  10 in total

1.  N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.

Authors:  E M Rinchik; D A Carpenter
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

2.  Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.

Authors:  Shahida Moosa; Guilherme L Yamamoto; Lutz Garbes; Katharina Keupp; Ana Beleza-Meireles; Carolina Araujo Moreno; Eugenia Ribeiro Valadares; Sérgio B de Sousa; Sofia Maia; Jorge Saraiva; Rachel S Honjo; Chong Ae Kim; Hamilton Cabral de Menezes; Ekkehart Lausch; Pablo Villavicencio Lorini; Arsonval Lamounier; Tulio Canella Bezerra Carniero; Cecilia Giunta; Marianne Rohrbach; Marco Janner; Oliver Semler; Filippo Beleggia; Yun Li; Gökhan Yigit; Nadine Reintjes; Janine Altmüller; Peter Nürnberg; Denise P Cavalcanti; Bernhard Zabel; Matthew L Warman; Debora R Bertola; Bernd Wollnik; Christian Netzer
Journal:  Am J Hum Genet       Date:  2019-09-26       Impact factor: 11.025

3.  Contemporary gene targeting strategies for the novice.

Authors:  S S Cheah; R R Behringer
Journal:  Mol Biotechnol       Date:  2001-11       Impact factor: 2.695

4.  MESD is essential for apical localization of megalin/LRP2 in the visceral endoderm.

Authors:  Janet K Lighthouse; Liqun Zhang; Jen-Chih Hsieh; Thomas Rosenquist; Bernadette C Holdener
Journal:  Dev Dyn       Date:  2010-11-08       Impact factor: 3.780

5.  The tumor suppressor gene Smad4/Dpc4 is required for gastrulation and later for anterior development of the mouse embryo.

Authors:  C Sirard; J L de la Pompa; A Elia; A Itie; C Mirtsos; A Cheung; S Hahn; A Wakeham; L Schwartz; S E Kern; J Rossant; T W Mak
Journal:  Genes Dev       Date:  1998-01-01       Impact factor: 11.361

Review 6.  An Update on Animal Models of Osteogenesis Imperfecta.

Authors:  Fang Lv; Xiaoling Cai; Linong Ji
Journal:  Calcif Tissue Int       Date:  2022-06-29       Impact factor: 4.000

7.  Suppression of Erk signalling promotes ground state pluripotency in the mouse embryo.

Authors:  Jennifer Nichols; Jose Silva; Mila Roode; Austin Smith
Journal:  Development       Date:  2009-08-26       Impact factor: 6.868

Review 8.  Osteogenesis Imperfecta: Mechanisms and Signaling Pathways Connecting Classical and Rare OI Types.

Authors:  Milena Jovanovic; Gali Guterman-Ram; Joan C Marini
Journal:  Endocr Rev       Date:  2022-01-12       Impact factor: 19.871

9.  Development of a conditional Mesd (mesoderm development) allele for functional analysis of the low-density lipoprotein receptor-related family in defined tissues.

Authors:  Andrew V Taibi; Janet K Lighthouse; Richard C Grady; Kenneth R Shroyer; Bernadette C Holdener
Journal:  PLoS One       Date:  2013-10-04       Impact factor: 3.240

10.  Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta.

Authors:  Thao T Tran; Rachel B Keller; Brecht Guillemyn; Melanie Pepin; Jane E Corteville; Samir Khatib; Mohammad-Sadegh Fallah; Sirous Zeinali; Fransiska Malfait; Sofie Symoens; Paul Coucke; Peter Witters; Elena Levtchenko; Hamideh Bagherian; Deborah A Nickerson; Michael J Bamshad; Jessica X Chong; Peter H Byers
Journal:  HGG Adv       Date:  2021-08-20
  10 in total

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