Literature DB >> 22903933

A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency.

Mohammad M Al-Qattan1, Ibrahim Al Abdulkareem, Yazied Al Haidan, Mohammed Al Balwi.   

Abstract

Sonic Hedgehog (SHH) within the posteriorly located zone of polarizing activity is the main controller of the antero-posterior axis of limb development. The ZRS (zone of polarizing activity regulatory sequence) is a long-range limb-specific SHH enhancer. Several point mutations in the ZRS have been described in humans. These mutations cause enhanced SHH activity and ectopic anterior expression of SHH and a variable phenotype of preaxial polydactyly and triphalangeal thumb. Absent thumb or radius has not been reported with ZRS mutations. Here, we report on a family with a variable phenotype of preaxial polydactyly as well as absent thumb and radius, with kidney and cardiac defects. The family was screened for SALL1, SALL4, and TBX5 mutations, but all were normal. Finally, they were screened for ZRS mutations, which showed a novel point mutation within the ZRS, NG_009240.1: g.106954C>T (traditional nomenclature: ZRS619C>T) in the five affected members. This mutation was not previously reported in any public domain database, and was not found in our healthy and ethnically matched control individuals or unaffected family members. We hypothesize that interactions of SHH and SALL1 explain the overlapping features of the family described here and patients with Townes-Brocks syndrome.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22903933     DOI: 10.1002/ajmg.a.35584

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  12 in total

1.  Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants.

Authors:  Evgeny Z Kvon; Yiwen Zhu; Guy Kelman; Catherine S Novak; Ingrid Plajzer-Frick; Momoe Kato; Tyler H Garvin; Quan Pham; Anne N Harrington; Riana D Hunter; Janeth Godoy; Eman M Meky; Jennifer A Akiyama; Veena Afzal; Stella Tran; Fabienne Escande; Brigitte Gilbert-Dussardier; Nolwenn Jean-Marçais; Sanjarbek Hudaiberdiev; Ivan Ovcharenko; Matthew B Dobbs; Christina A Gurnett; Sylvie Manouvrier-Hanu; Florence Petit; Axel Visel; Diane E Dickel; Len A Pennacchio
Journal:  Cell       Date:  2020-03-12       Impact factor: 41.582

2.  Alterations to the remote control of Shh gene expression cause congenital abnormalities.

Authors:  Robert E Hill; Laura A Lettice
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-05-06       Impact factor: 6.237

3.  Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome.

Authors:  Tomasz Zemojtel; Sebastian Köhler; Luisa Mackenroth; Marten Jäger; Jochen Hecht; Peter Krawitz; Luitgard Graul-Neumann; Sandra Doelken; Nadja Ehmke; Malte Spielmann; Nancy Christine Oien; Michal R Schweiger; Ulrike Krüger; Götz Frommer; Björn Fischer; Uwe Kornak; Ricarda Flöttmann; Amin Ardeshirdavani; Yves Moreau; Suzanna E Lewis; Melissa Haendel; Damian Smedley; Denise Horn; Stefan Mundlos; Peter N Robinson
Journal:  Sci Transl Med       Date:  2014-09-03       Impact factor: 17.956

Review 4.  Confirmation of genetic homogeneity of syndactyly type IV and triphalangeal thumb-polysyndactyly syndrome in a Chinese family and review of the literature.

Authors:  Limeng Dai; Hong Guo; Hui Meng; Kun Zhang; Hua Hu; Hong Yao; Yun Bai
Journal:  Eur J Pediatr       Date:  2013-06-22       Impact factor: 3.183

5.  Molecular signatures of selection on the human GLI3 associated central nervous system specific enhancers.

Authors:  Irfan Hussain; Rabail Zehra Raza; Shahid Ali; Muhammad Abrar; Amir Ali Abbasi
Journal:  Dev Genes Evol       Date:  2021-03-02       Impact factor: 0.900

6.  Hox5 interacts with Plzf to restrict Shh expression in the developing forelimb.

Authors:  Ben Xu; Steven M Hrycaj; Daniel C McIntyre; Nicholas C Baker; Jun K Takeuchi; Lucie Jeannotte; Zachary B Gaber; Bennett G Novitch; Deneen M Wellik
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-11       Impact factor: 11.205

Review 7.  Zone of Polarizing Activity Regulatory Sequence Mutations/Duplications with Preaxial Polydactyly and Longitudinal Preaxial Ray Deficiency in the Phenotype: A Review of Human Cases, Animal Models, and Insights Regarding the Pathogenesis.

Authors:  Mohammad M Al-Qattan
Journal:  Biomed Res Int       Date:  2018-02-13       Impact factor: 3.411

8.  Microduplication of 7q36.3 encompassing the SHH long‑range regulator (ZRS) in a patient with triphalangeal thumb‑polysyndactyly syndrome and congenital heart disease.

Authors:  Zhenghua Liu; Ni Yin; Lianghui Gong; Zhiping Tan; Bangliang Yin; Yifeng Yang; Cheng Luo
Journal:  Mol Med Rep       Date:  2016-12-29       Impact factor: 2.952

Review 9.  A multidisciplinary review of triphalangeal thumb.

Authors:  Jacob W P Potuijt; Robert-Jan H Galjaard; Peter J van der Spek; Christianne A van Nieuwenhoven; Nadav Ahituv; Kerby C Oberg; Steven E R Hovius
Journal:  J Hand Surg Eur Vol       Date:  2018-10-14

Review 10.  SHH Signaling Pathway Drives Pediatric Bone Sarcoma Progression.

Authors:  Frédéric Lézot; Isabelle Corre; Sarah Morice; Françoise Rédini; Franck Verrecchia
Journal:  Cells       Date:  2020-02-26       Impact factor: 6.600

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