Literature DB >> 26204134

Sodium/Iodide Symporter Mutant V270E Causes Stunted Growth but No Cognitive Deficiency.

Juan Pablo Nicola1, Andrea Reyna-Neyra1, Paul Saenger1, David F Rodriguez-Buritica1, José David Gamez Godoy1, Radhika Muzumdar1, L Mario Amzel1, Nancy Carrasco1.   

Abstract

CONTEXT: Iodide (I(-)), an essential constituent of the thyroid hormones, is actively accumulated in the thyroid by the Na(+)/I(-) symporter (NIS), a key plasma membrane protein encoded by the slc5a5 gene. Mutations in slc5a5 cause I(-) transport defects (ITDs), autosomal-recessive disorders in which I(-) accumulation is totally or partially impaired, leading to congenital hypothyroidism. The characterization of NIS mutants has yielded significant insights into the molecular mechanism of NIS.
OBJECTIVE: This study aimed to determine the basis of a patient's ITD clinical phenotype, by sequencing her slc5a5 gene.
DESIGN: Genomic DNA was purified and the slc5a5 gene sequence determined. Functional in vitro studies were performed to characterize the V270E NIS mutant. PATIENT: The index patient was diagnosed with hypothyroidism with minimal radioiodide uptake in a normally located, although enlarged, thyroid gland.
RESULTS: We identified a new NIS mutation: V270E. The patient had the compound heterozygous NIS mutation R124H/V270E. R124H NIS has been characterized previously. We show that V270E markedly reduces I(-) uptake via a pronounced (but not total) impairment of the protein's plasma membrane targeting. Remarkably, V270E is intrinsically active. Therefore, a negative charge at position 270 interferes with NIS cell surface trafficking. The patient's minimal I(-) uptake enabled sufficient thyroid hormone biosynthesis to prevent cognitive impairment.
CONCLUSIONS: A nonpolar residue at position 270, which all members of the SLC5A family have, is required for NIS plasma membrane targeting.

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Year:  2015        PMID: 26204134      PMCID: PMC4596044          DOI: 10.1210/jc.2015-1824

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  37 in total

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2.  Immunohistochemical profile of the sodium/iodide symporter in thyroid, breast, and other carcinomas using high density tissue microarrays and conventional sections.

Authors:  Irene L Wapnir; Matt van de Rijn; Kent Nowels; Peter S Amenta; Kelly Walton; Kelli Montgomery; Ralph S Greco; Orsolya Dohán; Nancy Carrasco
Journal:  J Clin Endocrinol Metab       Date:  2003-04       Impact factor: 5.958

3.  Na(+)-I- symport activity is present in membrane vesicles from thyrotropin-deprived non-I(-)-transporting cultured thyroid cells.

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Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-27       Impact factor: 11.205

8.  The Q267E mutation in the sodium/iodide symporter (NIS) causes congenital iodide transport defect (ITD) by decreasing the NIS turnover number.

Authors:  Antonio De La Vieja; Christopher S Ginter; Nancy Carrasco
Journal:  J Cell Sci       Date:  2004-01-20       Impact factor: 5.285

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Journal:  Nature       Date:  1996-02-01       Impact factor: 49.962

10.  Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.

Authors:  M G Martín; E Turk; M P Lostao; C Kerner; E M Wright
Journal:  Nat Genet       Date:  1996-02       Impact factor: 38.330

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  8 in total

Review 1.  The Sodium/Iodide Symporter (NIS): Molecular Physiology and Preclinical and Clinical Applications.

Authors:  Silvia Ravera; Andrea Reyna-Neyra; Giuseppe Ferrandino; L Mario Amzel; Nancy Carrasco
Journal:  Annu Rev Physiol       Date:  2017-02-10       Impact factor: 19.318

2.  Na+ coordination at the Na2 site of the Na+/I- symporter.

Authors:  Giuseppe Ferrandino; Juan Pablo Nicola; Yuly E Sánchez; Ignacia Echeverria; Yunlong Liu; L Mario Amzel; Nancy Carrasco
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3.  Silent but Not Harmless: A Synonymous SLC5A5 Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism.

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4.  A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.

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Journal:  J Clin Endocrinol Metab       Date:  2021-06-16       Impact factor: 5.958

5.  The Iodide Transport Defect-Causing Y348D Mutation in the Na+/I- Symporter Renders the Protein Intrinsically Inactive and Impairs Its Targeting to the Plasma Membrane.

Authors:  Andrea Reyna-Neyra; Lara Jung; Mayukh Chakrabarti; Mikel X Suárez; L Mario Amzel; Nancy Carrasco
Journal:  Thyroid       Date:  2021-06-04       Impact factor: 6.506

Review 6.  Genetic and Physiological Factors Affecting Human Milk Production and Composition.

Authors:  Yarden Golan; Yehuda G Assaraf
Journal:  Nutrients       Date:  2020-05-21       Impact factor: 5.717

7.  Novel Compound Heterozygous Pathogenic Mutations of SLC5A5 in a Chinese Patient With Congenital Hypothyroidism.

Authors:  Cao-Xu Zhang; Jun-Xiu Zhang; Liu Yang; Chang-Run Zhang; Feng Cheng; Rui-Jia Zhang; Ya Fang; Zheng Wang; Feng-Yao Wu; Pei-Zhang Li; Jun Liang; Rui Li; Huai-Dong Song
Journal:  Front Endocrinol (Lausanne)       Date:  2021-03-19       Impact factor: 5.555

8.  Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect.

Authors:  Carlos Eduardo Bernal Barquero; Romina Celeste Geysels; Virginie Jacques; Gerardo Hernán Carro; Mariano Martín; Victoria Peyret; María Celeste Abregú; Patricia Papendieck; Ana María Masini-Repiso; Frédérique Savagner; Ana Elena Chiesa; Cintia E Citterio; Juan Pablo Nicola
Journal:  Int J Mol Sci       Date:  2022-08-17       Impact factor: 6.208

  8 in total

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