Literature DB >> 33715275

The Mafb cleft-associated variant H131Q is not required for palatogenesis in the mouse.

Brian J Paul1, Kristina J Palmer2, Lindsey Rhea1, Melissa Carlson1, Jocelyn C Sharp2, C Herbert Pratt2, Stephen A Murray2, Martine Dunnwald1.   

Abstract

BACKGROUND: Orofacial clefts (OFCs) are common birth defects with complex etiology. Genome wide association studies for OFC have identified SNPs in and near MAFB. MAFB is a transcription factor critical for structural development of digits, kidneys, skin, and brain. MAFB is also expressed in the craniofacial region. Previous sequencing of MAFB in a Filipino population revealed a novel missense variant significantly associated with an increased risk for OFC. This MAFB variant, leading to the amino acid change H131Q, was knocked into the mouse Mafb, resulting in the MafbH131Q allele. The MafbH131Q construct was engineered to allow for deletion of Mafb ("Mafbdel ").
RESULTS: Mafbdel/del animals died shortly after birth. Conversely, MafbH131Q/H131Q mice survived into adulthood at Mendelian ratios. Mafbdel/del and MafbH131Q/H131Q heads exhibited normal macroscopic and histological appearance at all embryonic time points evaluated. The periderm was intact based on expression of keratin 6, p63, and E-cadherin. Despite no effect on craniofacial morphogenesis, H131Q inhibited the Mafb-dependent promoter activation of Arhgap29 in palatal mesenchymal, but not ectodermal-derived epithelial cells in a luciferase assay.
CONCLUSIONS: Mafb is dispensable for murine palatogenesis in vivo, and the cleft-associated variant H131Q, despite its lack of morphogenic effect, altered the expression of Arhgap29 in a cell-dependent context.
© 2021 American Association of Anatomists.

Entities:  

Keywords:  Mafb; craniofacial; development; mouse; mutation

Mesh:

Substances:

Year:  2021        PMID: 33715275      PMCID: PMC9266196          DOI: 10.1002/dvdy.327

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   2.842


  50 in total

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2.  A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

Authors:  Terri H Beaty; Jeffrey C Murray; Mary L Marazita; Ronald G Munger; Ingo Ruczinski; Jacqueline B Hetmanski; Kung Yee Liang; Tao Wu; Tanda Murray; M Daniele Fallin; Richard A Redett; Gerald Raymond; Holger Schwender; Sheng-Chih Jin; Margaret E Cooper; Martine Dunnwald; Maria A Mansilla; Elizabeth Leslie; Stephen Bullard; Andrew C Lidral; Lina M Moreno; Renato Menezes; Alexandre R Vieira; Aline Petrin; Allen J Wilcox; Rolv T Lie; Ethylin W Jabs; Yah Huei Wu-Chou; Philip K Chen; Hong Wang; Xiaoqian Ye; Shangzhi Huang; Vincent Yeow; Samuel S Chong; Sun Ha Jee; Bing Shi; Kaare Christensen; Mads Melbye; Kimberly F Doheny; Elizabeth W Pugh; Hua Ling; Eduardo E Castilla; Andrew E Czeizel; Lian Ma; L Leigh Field; Lawrence Brody; Faith Pangilinan; James L Mills; Anne M Molloy; Peadar N Kirke; John M Scott; James M Scott; Mauricio Arcos-Burgos; Alan F Scott
Journal:  Nat Genet       Date:  2010-05-02       Impact factor: 38.330

3.  Ectopic expression of the transcription factor MafB in basal keratinocytes induces hyperproliferation and perturbs epidermal homeostasis.

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Journal:  Exp Dermatol       Date:  2017-07-03       Impact factor: 3.960

4.  MEMO1 drives cranial endochondral ossification and palatogenesis.

Authors:  Eric Van Otterloo; Weiguo Feng; Kenneth L Jones; Nancy E Hynes; David E Clouthier; Lee Niswander; Trevor Williams
Journal:  Dev Biol       Date:  2015-12-31       Impact factor: 3.582

5.  A mutation in transcription factor MAFB causes Focal Segmental Glomerulosclerosis with Duane Retraction Syndrome.

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Journal:  Kidney Int       Date:  2018-05-18       Impact factor: 10.612

6.  Transforming growth factor-beta 3 is required for secondary palate fusion.

Authors:  G Proetzel; S A Pawlowski; M V Wiles; M Yin; G P Boivin; P N Howles; J Ding; M W Ferguson; T Doetschman
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

Review 7.  Long-range enhancer-promoter contacts in gene expression control.

Authors:  Stefan Schoenfelder; Peter Fraser
Journal:  Nat Rev Genet       Date:  2019-08       Impact factor: 53.242

8.  Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting.

Authors:  Huan Liu; Elizabeth J Leslie; Jenna C Carlson; Terri H Beaty; Mary L Marazita; Andrew C Lidral; Robert A Cornell
Journal:  Nat Commun       Date:  2017-03-13       Impact factor: 14.919

9.  Mafb and c-Maf Have Prenatal Compensatory and Postnatal Antagonistic Roles in Cortical Interneuron Fate and Function.

Authors:  Emily Ling-Lin Pai; Daniel Vogt; Alexandra Clemente-Perez; Gabriel L McKinsey; Frances S Cho; Jia Sheng Hu; Matt Wimer; Anirban Paul; Siavash Fazel Darbandi; Ramon Pla; Tomasz J Nowakowski; Lisa V Goodrich; Jeanne T Paz; John L R Rubenstein
Journal:  Cell Rep       Date:  2019-01-29       Impact factor: 9.423

10.  The Interaction of Genetic Background and Mutational Effects in Regulation of Mouse Craniofacial Shape.

Authors:  Christopher J Percival; Pauline Marangoni; Vagan Tapaltsyan; Ophir Klein; Benedikt Hallgrímsson
Journal:  G3 (Bethesda)       Date:  2017-05-05       Impact factor: 3.154

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