Literature DB >> 26041762

Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination.

Nadirah Damseh1, Alexandre Simonin2, Chaim Jalas3, Joseph A Picoraro4, Avraham Shaag5, Megan T Cho6, Barak Yaacov5, Julie Neidich7, Motee Al-Ashhab1, Jane Juusola7, Sherri Bale7, Aida Telegrafi7, Kyle Retterer7, John G Pappas8, Ellen Moran8, Joshua Cappell9, Kwame Anyane Yeboa4, Bassam Abu-Libdeh1, Matthias A Hediger2, Wendy K Chung10, Orly Elpeleg5, Simon Edvardson5.   

Abstract

BACKGROUND: L-serine plays an essential role in neuronal development and function. Although a non-essential amino acid, L-serine must be synthesised within the brain because of its poor permeability by the blood-brain barrier. Within the brain, its synthesis is confined to astrocytes, and its shuttle to neuronal cells is performed by a dedicated neutral amino acid transporter, ASCT1. METHODS AND
RESULTS: Using exome analysis we identified the recessive mutations, p.E256K, p.L315fs, and p.R457W, in SLC1A4, the gene encoding ASCT1, in patients with developmental delay, microcephaly and hypomyelination; seizure disorder was variably present. When expressed in a heterologous system, the mutations did not affect the protein level at the plasma membrane but abolished or markedly reduced L-serine transport for p.R457W and p.E256K mutations, respectively. Interestingly, p.E256K mutation displayed a lower L-serine and alanine affinity but the same substrate selectivity as wild-type ASCT1.
CONCLUSIONS: The clinical phenotype of ASCT1 deficiency is reminiscent of defects in L-serine biosynthesis. The data underscore that ASCT1 is essential in brain serine transport. The SLC1A4 p.E256K mutation has a carrier frequency of 0.7% in the Ashkenazi-Jewish population and should be added to the carrier screening panel in this community. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Molecular genetics; Neurology

Mesh:

Substances:

Year:  2015        PMID: 26041762     DOI: 10.1136/jmedgenet-2015-103104

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  21 in total

1.  Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.

Authors:  Myriam Srour; Fadi F Hamdan; Dianalee McKnight; Erica Davis; Hanna Mandel; Jeremy Schwartzentruber; Brissa Martin; Lysanne Patry; Christina Nassif; Alexandre Dionne-Laporte; Luis H Ospina; Emmanuelle Lemyre; Christine Massicotte; Rachel Laframboise; Bruno Maranda; Damian Labuda; Jean-Claude Décarie; Françoise Rypens; Dorith Goldsher; Catherine Fallet-Bianco; Jean-François Soucy; Anne-Marie Laberge; Catalina Maftei; Kym Boycott; Bernard Brais; Renée-Myriam Boucher; Guy A Rouleau; Nicholas Katsanis; Jacek Majewski; Orly Elpeleg; Mary K Kukolich; Stavit Shalev; Jacques L Michaud
Journal:  Am J Hum Genet       Date:  2015-10-17       Impact factor: 11.025

Review 2.  Genetic studies of alcohol dependence in the context of the addiction cycle.

Authors:  Matthew T Reilly; Antonio Noronha; David Goldman; George F Koob
Journal:  Neuropharmacology       Date:  2017-01-22       Impact factor: 5.250

3.  Novel European SLC1A4 variant: infantile spasms and population ancestry analysis.

Authors:  Judith Conroy; Nicholas M Allen; Kathleen Gorman; Eoghan O'Halloran; Amre Shahwan; Bryan Lynch; Sally A Lynch; Sean Ennis; Mary D King
Journal:  J Hum Genet       Date:  2016-05-19       Impact factor: 3.172

4.  On the phenotypic spectrum of serine biosynthesis defects.

Authors:  Ayman W El-Hattab; Ranad Shaheen; Jozef Hertecant; Hassan I Galadari; Badi S Albaqawi; Amira Nabil; Fowzan S Alkuraya
Journal:  J Inherit Metab Dis       Date:  2016-03-10       Impact factor: 4.982

5.  De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.

Authors:  Esther R Berko; Megan T Cho; Christine Eng; Yunru Shao; David A Sweetser; Jessica Waxler; Nathaniel H Robin; Fallon Brewer; Sandra Donkervoort; Payam Mohassel; Carsten G Bönnemann; Martin Bialer; Christine Moore; Lynne A Wolfe; Cynthia J Tifft; Yufeng Shen; Kyle Retterer; Francisca Millan; Wendy K Chung
Journal:  J Med Genet       Date:  2016-07-07       Impact factor: 6.318

Review 6.  Epilepsy in inherited neurotransmitter disorders: Spotlights on pathophysiology and clinical management.

Authors:  Mario Mastrangelo
Journal:  Metab Brain Dis       Date:  2020-10-23       Impact factor: 3.584

7.  Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination.

Authors:  Tamar Harel; Debra Q Y Quek; Bernice H Wong; Amaury Cazenave-Gassiot; Markus R Wenk; Hao Fan; Itai Berger; Dorit Shmueli; Avraham Shaag; David L Silver; Orly Elpeleg; Shimon Edvardson
Journal:  Neurogenetics       Date:  2018-07-24       Impact factor: 2.660

8.  ASCT1 (Slc1a4) transporter is a physiologic regulator of brain d-serine and neurodevelopment.

Authors:  Eitan Kaplan; Salman Zubedat; Inna Radzishevsky; Alec C Valenta; Ohad Rechnitz; Hagit Sason; Clara Sajrawi; Oded Bodner; Kohtarou Konno; Kayoko Esaki; Dori Derdikman; Takeo Yoshikawa; Masahiko Watanabe; Robert T Kennedy; Jean-Marie Billard; Avi Avital; Herman Wolosker
Journal:  Proc Natl Acad Sci U S A       Date:  2018-09-05       Impact factor: 11.205

Review 9.  Functional and Biochemical Consequences of Disease Variants in Neurotransmitter Transporters: A Special Emphasis on Folding and Trafficking Deficits.

Authors:  Shreyas Bhat; Ali El-Kasaby; Michael Freissmuth; Sonja Sucic
Journal:  Pharmacol Ther       Date:  2020-12-10       Impact factor: 12.310

10.  Clinical application of whole-exome sequencing across clinical indications.

Authors:  Kyle Retterer; Jane Juusola; Megan T Cho; Patrik Vitazka; Francisca Millan; Federica Gibellini; Annette Vertino-Bell; Nizar Smaoui; Julie Neidich; Kristin G Monaghan; Dianalee McKnight; Renkui Bai; Sharon Suchy; Bethany Friedman; Jackie Tahiliani; Daniel Pineda-Alvarez; Gabriele Richard; Tracy Brandt; Eden Haverfield; Wendy K Chung; Sherri Bale
Journal:  Genet Med       Date:  2015-12-03       Impact factor: 8.822

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