ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type

Tatsuya Furuichi, Hiroshi Masuya, Tomohiko Murakami, Keiichiro Nishida, Gen Nishimura, Tomohiro Suzuki, Kazunori Imaizumi, Takashi Kudo, Kiyoshi Ohkawa, Shigeharu Wakana, Shiro Ikegawa

Research output: Contribution to journalArticle

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Abstract

The COL2A1 gene encodes the a1(II) chain of the homotrimeric type II collagen, the most abundant protein in cartilage. In humans, COL2A1 mutations create many clinical phenotypes collectively termed type II collagenopathies; however, the genetic basis of the phenotypic diversity is not well elucidated. Therefore, animal models corresponding to multiple type II collagenopathies are required. In this study we identified a novel Col2a1 missense mutation-c.44406A>C (p.D1469A)-produced by large-scale N-ethyl-N-nitrosourea (ENU) mutagenesis in a mouse line. This mutation was located in the C-propeptide coding region of Col2a1 and in the positions corresponding to a human COL2A1 mutation responsible for platyspondylic lethal skeletal dysplasia, Torrance type (PLSD-T). The phenotype was inherited as a semidominant trait. The heterozygotes were mildly but significantly smaller than wild-type mice. The homozygotes exhibited lethal skeletal dysplasias, including extremely short limbs, severe spondylar dysplasia, severe pelvic hypoplasia, and brachydactyly. As expected, these skeletal defects in the homozygotes were similar to those in PLSD-T patients. The secretion of the mutant proteins into the extracellular space was disrupted, accompanied by abnormally expanded rough endoplasmic reticulum (ER) and upregulation of ER stress-related genes, such as Grp94 and Chop, in chondrocytes. These findings suggested that the accumulation of mutant type II collagen in the ER and subsequent induction of ER stress are involved, at least in part in the PLSD-T-like phenotypes of the mutants. This mutant should serve as a good model for studying PLSD-T pathogenesis and the mechanisms that create the great diversity of type II collagenopathies.

Original languageEnglish
Pages (from-to)318-328
Number of pages11
JournalMammalian Genome
Volume22
Issue number5-6
DOIs
Publication statusPublished - Jun 2011

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Missense Mutation
Endoplasmic Reticulum Stress
Collagen Type II
Homozygote
Phenotype
Mutation
Brachydactyly
Ethylnitrosourea
Rough Endoplasmic Reticulum
Extracellular Space
Mutant Proteins
Heterozygote
Chondrocytes
Mutagenesis
Endoplasmic Reticulum
Genes
Cartilage
Up-Regulation
Extremities
Animal Models

ASJC Scopus subject areas

  • Genetics

Cite this

ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type. / Furuichi, Tatsuya; Masuya, Hiroshi; Murakami, Tomohiko; Nishida, Keiichiro; Nishimura, Gen; Suzuki, Tomohiro; Imaizumi, Kazunori; Kudo, Takashi; Ohkawa, Kiyoshi; Wakana, Shigeharu; Ikegawa, Shiro.

In: Mammalian Genome, Vol. 22, No. 5-6, 06.2011, p. 318-328.

Research output: Contribution to journalArticle

Furuichi, T, Masuya, H, Murakami, T, Nishida, K, Nishimura, G, Suzuki, T, Imaizumi, K, Kudo, T, Ohkawa, K, Wakana, S & Ikegawa, S 2011, 'ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type', Mammalian Genome, vol. 22, no. 5-6, pp. 318-328. https://doi.org/10.1007/s00335-011-9329-3
Furuichi, Tatsuya ; Masuya, Hiroshi ; Murakami, Tomohiko ; Nishida, Keiichiro ; Nishimura, Gen ; Suzuki, Tomohiro ; Imaizumi, Kazunori ; Kudo, Takashi ; Ohkawa, Kiyoshi ; Wakana, Shigeharu ; Ikegawa, Shiro. / ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type. In: Mammalian Genome. 2011 ; Vol. 22, No. 5-6. pp. 318-328.
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