Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion

Authors

  • SA Boyadjiev,

    Corresponding author
    1. Section of Genetics, Department of Pediatrics, University of California Davis Medical Center, Sacramento, CA, USA
      Simeon A. Boyadjiev and Jinoh Kim, 2805 50th Street, MIND Institute, Wet laboratory 1421, Sacramento, CA 95618, USA.
      Tel.: +916 703 0451;
      Fax: +916 703 0370;
      e-mail: simeon.boyd@ucdmc.ucdavis.edu; jinoh.kim@ucdmc.ucdavis.edu
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  • S-D Kim,

    1. Section of Genetics, Department of Pediatrics, University of California Davis Medical Center, Sacramento, CA, USA
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  • A Hata,

    1. Section of Genetics, Department of Pediatrics, University of California Davis Medical Center, Sacramento, CA, USA
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  • C Haldeman-Englert,

    1. Section on Medical Genetics, Department of Pediatrics, Wake Forest University School of Medicine, Winston-Salem, NC, USA
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  • EH Zackai,

    1. Division of Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, PA, USA
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  • C Naydenov,

    1. Department of Chemistry and Biochemistry, Medical University, Sofia, Bulgaria
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  • S Hamamoto,

    1. Department of Molecular and Cell Biology, Howard Hughes Medical Institute, University of California, Berkeley, CA, USA
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  • RW Schekman,

    1. Department of Molecular and Cell Biology, Howard Hughes Medical Institute, University of California, Berkeley, CA, USA
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  • J Kim

    Corresponding author
    1. Section of Genetics, Department of Pediatrics, University of California Davis Medical Center, Sacramento, CA, USA
      Simeon A. Boyadjiev and Jinoh Kim, 2805 50th Street, MIND Institute, Wet laboratory 1421, Sacramento, CA 95618, USA.
      Tel.: +916 703 0451;
      Fax: +916 703 0370;
      e-mail: simeon.boyd@ucdmc.ucdavis.edu; jinoh.kim@ucdmc.ucdavis.edu
    Search for more papers by this author

Simeon A. Boyadjiev and Jinoh Kim, 2805 50th Street, MIND Institute, Wet laboratory 1421, Sacramento, CA 95618, USA.
Tel.: +916 703 0451;
Fax: +916 703 0370;
e-mail: simeon.boyd@ucdmc.ucdavis.edu; jinoh.kim@ucdmc.ucdavis.edu

Abstract

Boyadjiev SA, Kim S-D, Hata A, Haldeman-Englert C, Zackai EH, Naydenov C, Hamamoto S, Schekman RW, Kim J. Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion.

Cranio-lenticulo-sutural dysplasia (CLSD) is a rare autosomal recessive syndrome manifesting with large and late-closing fontanels and calvarial hypomineralization, Y-shaped cataracts, skeletal defects, and hypertelorism and other facial dysmorphisms. The CLSD locus was mapped to chromosome 14q13-q21 and a homozygous SEC23A F382L missense mutation was identified in the original family. Skin fibroblasts from these patients exhibit features of a secretion defect with marked distension of the endoplasmic reticulum (ER), consistent with SEC23A function in protein export from the ER. We report an unrelated family where a male proband presented with clinical features of CLSD. A heterozygous missense M702V mutation in a highly conserved residue of SEC23A was inherited from the clinically unaffected father, but no maternal SEC23A mutation was identified. Cultured skin fibroblasts from this new patient showed a severe secretion defect of collagen and enlarged ER, confirming aberrant protein export from the ER. Milder collagen secretion defects and ER distention were present in paternal fibroblasts, indicating that an additional mutation(s) is present in the proband. Our data suggest that defective ER export is the cause of CLSD and genetic element(s) besides SEC23A may influence its presentation.

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