Literature DB >> 30219651

Fibrillin protein pleiotropy: Acromelic dysplasias.

Lynn Y Sakai1, Douglas R Keene2.   

Abstract

The fibrillins are large extracellular matrix molecules that polymerize to form microfibrils. Fibrillin microfibrils are distinctive architectural elements that are both ubiquitous in the connective tissue space and also unique, displaying tissue-specific patterns. Mutations in the genes for fibrillin-1 (FBN1) result in multiple distinct pleiotropic disorders. Most of the more than 3000 mutations known today in FBN1 cause the Marfan syndrome. Marfan mutations can occur in any of the 56 domains that compose fibrillin-1. In contrast, rare mutations in FBN1 that are confined to only certain domains cause several different types of acromelic dysplasia. These genetic disorders demonstrate that specific domains of fibrillin-1 perform roles important to musculoskeletal growth. Many of the phenotypes of acromelic dysplasias are the opposite of those found in Marfan syndrome. Knowledge of the functions and structural organization of fibrillin molecules within microfibrils is required to understand how one protein and one gene can be the basis for multiple genetic disorders.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acromicric dysplasia; Fibrillin; Geleophysic dysplasia; Stiff Skin Syndrome; Weill-Marchesani syndrome

Mesh:

Substances:

Year:  2018        PMID: 30219651     DOI: 10.1016/j.matbio.2018.09.005

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  13 in total

1.  Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia.

Authors:  Dirk Hubmacher; Nandaraj Taye; Zerina Balic; Stetson Thacker; Sheila M Adams; David E Birk; Ronen Schweitzer; Suneel S Apte
Journal:  Matrix Biol       Date:  2019-02-07       Impact factor: 11.583

2.  Adamts17 is involved in skeletogenesis through modulation of BMP-Smad1/5/8 pathway.

Authors:  Takeshi Oichi; Yuki Taniguchi; Kazuhito Soma; Yasushi Oshima; Fumiko Yano; Yoshifumi Mori; Ryota Chijimatsu; Joo-Ri Kim-Kaneyama; Sakae Tanaka; Taku Saito
Journal:  Cell Mol Life Sci       Date:  2019-06-14       Impact factor: 9.261

Review 3.  The "other" 15-40%: The Role of Non-Collagenous Extracellular Matrix Proteins and Minor Collagens in Tendon.

Authors:  Nandaraj Taye; Stylianos Z Karoulias; Dirk Hubmacher
Journal:  J Orthop Res       Date:  2019-08-26       Impact factor: 3.494

4.  Fibrillin-1 deficiency in the outer perichondrium causes longitudinal bone overgrowth in mice with Marfan syndrome.

Authors:  Lauriane Sedes; Elisa Wondimu; Brittany Crockett; Jens Hansen; Anna Cantalupo; Keiichi Asano; Ravi Iyengar; Daniel B Rifkin; Silvia Smaldone; Francesco Ramirez
Journal:  Hum Mol Genet       Date:  2022-09-29       Impact factor: 5.121

5.  Genetic regulation of linear growth.

Authors:  Shanna Yue; Philip Whalen; Youn Hee Jee
Journal:  Ann Pediatr Endocrinol Metab       Date:  2019-03-31

6.  Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1-Related Disorders.

Authors:  Carmela Fusco; Silvia Morlino; Lucia Micale; Alessandro Ferraris; Paola Grammatico; Marco Castori
Journal:  Genes (Basel)       Date:  2019-06-10       Impact factor: 4.096

7.  Novel p.G1344E mutation in FBN1 is associated with ectopia lentis.

Authors:  Yuan Yang; Ya-Li Zhou; Teng-Teng Yao; Hui Pan; Ping Gu; Zhao-Yang Wang
Journal:  Br J Ophthalmol       Date:  2020-05-13       Impact factor: 4.638

8.  Acromelic dysplasias: how rare musculoskeletal disorders reveal biological functions of extracellular matrix proteins.

Authors:  Sarah Stanley; Zerina Balic; Dirk Hubmacher
Journal:  Ann N Y Acad Sci       Date:  2020-09-02       Impact factor: 5.691

Review 9.  The ADAMTS/Fibrillin Connection: Insights into the Biological Functions of ADAMTS10 and ADAMTS17 and Their Respective Sister Proteases.

Authors:  Stylianos Z Karoulias; Nandaraj Taye; Sarah Stanley; Dirk Hubmacher
Journal:  Biomolecules       Date:  2020-04-12

10.  A Review of Three Chinese Cases of Acromicric/Geleophysic Dysplasia with FBN1 Mutations.

Authors:  Yan-Chun Shan; Zhao-Chuan Yang; Liang Ma; Ni Ran; Xue-Ying Feng; Xiao-Mei Liu; Peng Fu; Ming-Ji Yi
Journal:  Int J Gen Med       Date:  2021-05-17
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