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Somatic uniparental disomy mitigates the most damaging EFL1 allele combination in Shwachman-Diamond syndrome.
Lee, Sangmoon; Shin, Chang Hoon; Lee, Jawon; Jeong, Seong Dong; Hong, Che Ry; Kim, Jun-Dae; Kim, Ah-Ra; Park, Boryeong; Son, Soo Jin; Kokhan, Oleksandr; Yoo, Taekyeong; Ko, Jae Sung; Sohn, Young Bae; Kim, Ok-Hwa; Ko, Jung Min; Cho, Tae-Joon; Wright, Nathan T; Seong, Je Kyung; Jin, Suk-Won; Kang, Hyoung Jin; Kim, Hyeon Ho; Choi, Murim.
Affiliation
  • Lee S; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
  • Shin CH; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South Korea.
  • Lee J; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
  • Jeong SD; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South Korea.
  • Hong CR; Department of Pediatrics, Seoul National University College of Medicine, Seoul, South Korea.
  • Kim JD; Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT.
  • Kim AR; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, South Korea.
  • Park B; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, South Korea.
  • Son SJ; Laboratory of Developmental Biology and Genomics, Research Institute for Veterinary Science, and BK21 PLUS Program for Creative Veterinary Science Research, College of Veterinary Medicine, and.
  • Kokhan O; Korea Mouse Phenotyping Center, Seoul National University, Seoul, South Korea.
  • Yoo T; Department of Chemistry and Biochemistry, James Madison University, Harrisonburg, VA.
  • Ko JS; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
  • Sohn YB; Department of Pediatrics, Seoul National University College of Medicine, Seoul, South Korea.
  • Kim OH; Department of Medical Genetics, Ajou University Hospital, Ajou University School of Medicine, Suwon, South Korea.
  • Ko JM; Department of Pediatric Radiology, VIC 365 Children's Hospital, Incheon, South Korea.
  • Cho TJ; Department of Pediatrics, Seoul National University College of Medicine, Seoul, South Korea.
  • Wright NT; Department of Orthopaedic Surgery, Seoul National University College of Medicine, Seoul, South Korea.
  • Seong JK; Department of Chemistry and Biochemistry, James Madison University, Harrisonburg, VA.
  • Jin SW; Laboratory of Developmental Biology and Genomics, Research Institute for Veterinary Science, and BK21 PLUS Program for Creative Veterinary Science Research, College of Veterinary Medicine, and.
  • Kang HJ; Korea Mouse Phenotyping Center, Seoul National University, Seoul, South Korea.
  • Kim HH; Interdisciplinary Program for Bioinformatics-Program for Cancer Biology, BIO-MAX/N-Bio Institute, Seoul National University, Seoul, South Korea.
  • Choi M; Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT.
Blood ; 138(21): 2117-2128, 2021 11 25.
Article in En | MEDLINE | ID: mdl-34115847
Shwachman-Diamond syndrome (SDS; OMIM #260400) is caused by variants in SBDS (Shwachman-Bodian-Diamond syndrome gene), which encodes a protein that plays an important role in ribosome assembly. Recent reports suggest that recessive variants in EFL1 are also responsible for SDS. However, the precise genetic mechanism that leads to EFL1-induced SDS remains incompletely understood. Here we present 3 unrelated Korean SDS patients who carry biallelic pathogenic variants in EFL1 with biased allele frequencies, resulting from a bone marrow-specific somatic uniparental disomy in chromosome 15. The recombination events generated cells that were homozygous for the relatively milder variant, allowing for the evasion of catastrophic physiologic consequences. However, the milder EFL1 variant was still solely able to impair 80S ribosome assembly and induce SDS features in cell line and animal models. The loss of EFL1 resulted in a pronounced inhibition of terminal oligopyrimidine element-containing ribosomal protein transcript 80S assembly. Therefore, we propose a more accurate pathogenesis mechanism of EFL1 dysfunction that eventually leads to aberrant translational control and ribosomopathy.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Elongation Factors / Ribonucleoprotein, U5 Small Nuclear / Uniparental Disomy / Shwachman-Diamond Syndrome Type of study: Prognostic_studies Limits: Adult / Animals / Child / Child, preschool / Female / Humans / Male Language: En Journal: Blood Year: 2021 Document type: Article Affiliation country: Korea (South) Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Elongation Factors / Ribonucleoprotein, U5 Small Nuclear / Uniparental Disomy / Shwachman-Diamond Syndrome Type of study: Prognostic_studies Limits: Adult / Animals / Child / Child, preschool / Female / Humans / Male Language: En Journal: Blood Year: 2021 Document type: Article Affiliation country: Korea (South) Country of publication: United States