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Transcriptional Determinism and Stochasticity Contribute to the Complexity of Autism Associated SHANK Family Genes.
Lu, Xiaona; Ni, Pengyu; Suarez-Meade, Paola; Ma, Yu; Forrest, Emily Niemitz; Wang, Guilin; Wang, Yi; Quiñones-Hinojosa, Alfredo; Gerstein, Mark; Jiang, Yong-Hui.
Afiliação
  • Lu X; Department of Genetics, Yale University School of Medicine New Haven, CT, 06520 USA.
  • Ni P; Biomedical Informatics & Data Science, Yale University School of Medicine New Haven, CT, 06520 USA.
  • Suarez-Meade P; Department of Neurosurgery, Mayo Clinic, Jacksonville, FL, 32224 USA.
  • Ma Y; Department of Neurology, Children's Hospital of Fudan University, Shanghai, 201102 China.
  • Forrest EN; Department of Genetics, Yale University School of Medicine New Haven, CT, 06520 USA.
  • Wang G; Yale Center for Genome Analysis, Yale University School of Medicine New Haven, CT, 06520 USA.
  • Wang Y; Department of Neurology, Children's Hospital of Fudan University, Shanghai, 201102 China.
  • Quiñones-Hinojosa A; Department of Neurosurgery, Mayo Clinic, Jacksonville, FL, 32224 USA.
  • Gerstein M; Biomedical Informatics & Data Science, Yale University School of Medicine New Haven, CT, 06520 USA.
  • Jiang YH; Yale Center for Genome Analysis, Yale University School of Medicine New Haven, CT, 06520 USA.
bioRxiv ; 2024 Mar 19.
Article em En | MEDLINE | ID: mdl-38562714
ABSTRACT
Precision of transcription is critical because transcriptional dysregulation is disease causing. Traditional methods of transcriptional profiling are inadequate to elucidate the full spectrum of the transcriptome, particularly for longer and less abundant mRNAs. SHANK3 is one of the most common autism causative genes. Twenty-four Shank3 mutant animal lines have been developed for autism modeling. However, their preclinical validity has been questioned due to incomplete Shank3 transcript structure. We applied an integrative approach combining cDNA-capture and long-read sequencing to profile the SHANK3 transcriptome in human and mice. We unexpectedly discovered an extremely complex SHANK3 transcriptome. Specific SHANK3 transcripts were altered in Shank3 mutant mice and postmortem brains tissues from individuals with ASD. The enhanced SHANK3 transcriptome significantly improved the detection rate for potential deleterious variants from genomics studies of neuropsychiatric disorders. Our findings suggest the stochastic transcription of genome associated with SHANK family genes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article