Literature DB >> 32969791

MondoA regulates gene expression in cholesterol biosynthesis-associated pathways required for zebrafish epiboly.

Meltem Weger1,2,3, Benjamin D Weger1,3,4, Andrea Schink1, Masanari Takamiya1, Johannes Stegmaier5, Cédric Gobet4, Alice Parisi4, Andrei Yu Kobitski1,6, Jonas Mertes6, Nils Krone2, Uwe Strähle1, Gerd Ulrich Nienhaus1,6,7,8, Ralf Mikut5, Frédéric Gachon3,4, Philipp Gut4, Thomas Dickmeis1.   

Abstract

The glucose-sensing Mondo pathway regulates expression of metabolic genes in mammals. Here, we characterized its function in the zebrafish and revealed an unexpected role of this pathway in vertebrate embryonic development. We showed that knockdown of mondoa impaired the early morphogenetic movement of epiboly in zebrafish embryos and caused microtubule defects. Expression of genes in the terpenoid backbone and sterol biosynthesis pathways upstream of pregnenolone synthesis was coordinately downregulated in these embryos, including the most downregulated gene nsdhl. Loss of Nsdhl function likewise impaired epiboly, similar to MondoA loss of function. Both epiboly and microtubule defects were partially restored by pregnenolone treatment. Maternal-zygotic mutants of mondoa showed perturbed epiboly with low penetrance and compensatory changes in the expression of terpenoid/sterol/steroid metabolism genes. Collectively, our results show a novel role for MondoA in the regulation of early vertebrate development, connecting glucose, cholesterol and steroid hormone metabolism with early embryonic cell movements.
© 2020, Weger et al.

Entities:  

Keywords:  carbohydrate response element; cholesterol; developmental biology; epiboly; genetics; genomics; metabolism; microtubule; pregnenolone; zebrafish

Mesh:

Substances:

Year:  2020        PMID: 32969791      PMCID: PMC7515633          DOI: 10.7554/eLife.57068

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


  106 in total

1.  Glucose 6-phosphate, rather than xylulose 5-phosphate, is required for the activation of ChREBP in response to glucose in the liver.

Authors:  Renaud Dentin; Lidia Tomas-Cobos; Fabienne Foufelle; Jane Leopold; Jean Girard; Catherine Postic; Pascal Ferré
Journal:  J Hepatol       Date:  2011-08-09       Impact factor: 25.083

2.  Patterning the early zebrafish by the opposing actions of bozozok and vox/vent.

Authors:  A E Melby; C Beach; M Mullins; D Kimelman
Journal:  Dev Biol       Date:  2000-08-15       Impact factor: 3.582

3.  Glucose sensing by MondoA:Mlx complexes: a role for hexokinases and direct regulation of thioredoxin-interacting protein expression.

Authors:  Carrie A Stoltzman; Christopher W Peterson; Kevin T Breen; Deborah M Muoio; Andrew N Billin; Donald E Ayer
Journal:  Proc Natl Acad Sci U S A       Date:  2008-05-05       Impact factor: 11.205

4.  Enzymatic assays for 2-deoxyglucose and 2-deoxyglucose 6-phosphate.

Authors:  M M Chi; M E Pusateri; J G Carter; B J Norris; D B McDougal; O H Lowry
Journal:  Anal Biochem       Date:  1987-03       Impact factor: 3.365

5.  Discovery of a functional glucocorticoid receptor beta-isoform in zebrafish.

Authors:  Marcel J M Schaaf; Danielle Champagne; Ivo H C van Laanen; Diane C W A van Wijk; Annemarie H Meijer; Onno C Meijer; Herman P Spaink; Michael K Richardson
Journal:  Endocrinology       Date:  2007-12-20       Impact factor: 4.736

6.  Manipulation of CD98 expression affects both trophoblast cell fusion and amino acid transport activity during syncytialization of human placental BeWo cells.

Authors:  Yoshiki Kudo; C A R Boyd; J Millo; I L Sargent; C W G Redman
Journal:  J Physiol       Date:  2003-05-09       Impact factor: 5.182

7.  Integrated expression profiling and genome-wide analysis of ChREBP targets reveals the dual role for ChREBP in glucose-regulated gene expression.

Authors:  Yun-Seung Jeong; Deokhoon Kim; Yong Seok Lee; Ha-Jung Kim; Jung-Youn Han; Seung-Soon Im; Hansook Kim Chong; Je-Keun Kwon; Yun-Ho Cho; Woo Kyung Kim; Timothy F Osborne; Jay D Horton; Hee-Sook Jun; Yong-Ho Ahn; Sung-Min Ahn; Ji-Young Cha
Journal:  PLoS One       Date:  2011-07-21       Impact factor: 3.240

8.  Cellular acidosis triggers human MondoA transcriptional activity by driving mitochondrial ATP production.

Authors:  Blake R Wilde; Zhizhou Ye; Tian-Yeh Lim; Donald E Ayer
Journal:  Elife       Date:  2019-02-05       Impact factor: 8.140

9.  Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish.

Authors:  S E Stachel; D J Grunwald; P Z Myers
Journal:  Development       Date:  1993-04       Impact factor: 6.868

Review 10.  Glucose-Sensing Transcription Factor MondoA/ChREBP as Targets for Type 2 Diabetes: Opportunities and Challenges.

Authors:  Ziyi Song; Hao Yang; Lei Zhou; Fajun Yang
Journal:  Int J Mol Sci       Date:  2019-10-16       Impact factor: 5.923

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