Genetic dissection of the Down syndrome critical region

Xiaoling Jiang, Chunhong Liu, Tao Yu, Li Zhang, Kai Meng, Zhuo Xing, Pavel V. Belichenko, Alexander M. Kleschevnikov, Annie Pao, Jennifer Peresie, Sarah Wie, William C. Mobley, Y. Eugene Yu

Research output: Contribution to journalArticle

Abstract

Down syndrome (DS), caused by trisomy 21, is the most common chromosomal disorder associated with developmental cognitive deficits. Despite intensive efforts, the genetic mechanisms underlying developmental cognitive deficits remain poorly understood, and no treatment has been proven effective. The previous mouse-based experiments suggest that the so-called Down syndrome critical region of human chromosome 21 is an important region for this phenotype, which is demarcated by Setd4/Cbr1 and Fam3b/Mx2. We first confirmed the importance of the Cbr1-Fam3b region using compound mutant mice, which carry a duplication spanning the entire human chromosome 21 orthologous region on mouse chromosome 16 [Dp(16)1Yey] and Ms1Rhr. By dividing the Setd4-Mx2 region into complementary Setd4-Kcnj6 and Kcnj15-Mx2 intervals, we started an unbiased dissection through generating and analyzing Dp(16)1Yey/Df(16Setd4-Kcnj6)Yey and Dp(16)1Yey/Df(16Kcnj15-Mx2)Yey mice. Surprisingly, the Dp(16)1Yey-associated cognitive phenotypes were not rescued by either deletion in the compound mutants, suggesting the possible presence of at least one causative gene in each of the two regions. The partial rescue by a Dyrk1a mutation in a compound mutant carrying Dp(16)1Yey and the Dyrk1a mutation confirmed the causative role of Dyrk1a, whereas the absence of a similar rescue by Df(16Dyrk1a-Kcnj6)Yey in Dp(16)1Yey/Df(16Dyrk1a-Kcnj6)Yey mice demonstrated the importance of Kcnj6. Our results revealed the high levels of complexities of gene actions and interactions associated with the Setd4/Cbr1-Fam3b/Mx2 region as well as their relationship with developmental cognitive deficits in DS.

Original languageEnglish (US)
Pages (from-to)6540-6551
Number of pages12
JournalHuman Molecular Genetics
Volume24
Issue number22
DOIs
StatePublished - 2015
Externally publishedYes

Fingerprint

Dissection
Down Syndrome
Chromosomes, Human, Pair 21
Human Chromosomes
Chromosome Disorders
Phenotype
Chromosomes, Human, Pair 16
Mutation
Genes
Down Syndrome Critical Region

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)
  • Molecular Biology

Cite this

Jiang, X., Liu, C., Yu, T., Zhang, L., Meng, K., Xing, Z., ... Yu, Y. E. (2015). Genetic dissection of the Down syndrome critical region. Human Molecular Genetics, 24(22), 6540-6551. https://doi.org/10.1093/hmg/ddv364

Genetic dissection of the Down syndrome critical region. / Jiang, Xiaoling; Liu, Chunhong; Yu, Tao; Zhang, Li; Meng, Kai; Xing, Zhuo; Belichenko, Pavel V.; Kleschevnikov, Alexander M.; Pao, Annie; Peresie, Jennifer; Wie, Sarah; Mobley, William C.; Yu, Y. Eugene.

In: Human Molecular Genetics, Vol. 24, No. 22, 2015, p. 6540-6551.

Research output: Contribution to journalArticle

Jiang, X, Liu, C, Yu, T, Zhang, L, Meng, K, Xing, Z, Belichenko, PV, Kleschevnikov, AM, Pao, A, Peresie, J, Wie, S, Mobley, WC & Yu, YE 2015, 'Genetic dissection of the Down syndrome critical region', Human Molecular Genetics, vol. 24, no. 22, pp. 6540-6551. https://doi.org/10.1093/hmg/ddv364
Jiang, Xiaoling ; Liu, Chunhong ; Yu, Tao ; Zhang, Li ; Meng, Kai ; Xing, Zhuo ; Belichenko, Pavel V. ; Kleschevnikov, Alexander M. ; Pao, Annie ; Peresie, Jennifer ; Wie, Sarah ; Mobley, William C. ; Yu, Y. Eugene. / Genetic dissection of the Down syndrome critical region. In: Human Molecular Genetics. 2015 ; Vol. 24, No. 22. pp. 6540-6551.
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AU - Zhang, Li

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AU - Belichenko, Pavel V.

AU - Kleschevnikov, Alexander M.

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AU - Yu, Y. Eugene

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