Iwanami Norimasa, Takahama Yousuke, Kunimatsu Sanae, Li Jie, Takei Rie, Ishikura Yuko, Suwa Hiroshi, Niwa Katsutoshi, Sasado Takao, Morinaga Chikako, Yasuoka Akihito, Deguchi Tomonori, Hirose Yukihiro, Yoda Hiroki, Henrich Thorsten, Ohara Osamu, Kondoh Hisato, Furutani-Seiki Makoto
Division of Experimental Immunology, Institute for Genome Research, University of Tokushima, 3-18-15 Kuramoto, Tokushima 770-8503, Japan.
Mech Dev. 2004 Jul;121(7-8):779-89. doi: 10.1016/j.mod.2004.03.020.
The thymus is an organ for T lymphocyte maturation and is indispensable for the establishment of a highly developed immune system in vertebrates. In order to genetically dissect thymus organogenesis, we carried out a large-scale mutagenesis screening for Medaka mutations affecting recombination activating gene 1 (rag1) expression in the developing thymus. We identified 24 mutations, defining at least 13 genes, which led to a marked reduction of rag1 expression in the thymus. As thymus development depends on pharyngeal arches, we classified those mutations into three classes according to the defects in the pharyngeal arches. Class 1 mutants had no or slight morphological abnormalities in the pharyngeal arches, implying that the mutations may include defects in such thymus-specific events as lymphocyte development and thymic epithelial cell maturation. Class 2 mutants had abnormally shaped pharyngeal arches. Class 3 mutants showed severely attenuated pharyngeal arch development. In Class 2 and Class 3 mutants, the defects in thymus development may be due to abnormal pharyngeal arch development. Those mutations are expected to be useful for identifying the molecular mechanisms underlying thymus organogenesis.
胸腺是T淋巴细胞成熟的器官,对于脊椎动物建立高度发达的免疫系统不可或缺。为了从基因层面剖析胸腺器官发生过程,我们对影响发育中胸腺内重组激活基因1(rag1)表达的青鳉突变体进行了大规模诱变筛选。我们鉴定出24个突变,定义了至少13个基因,这些突变导致胸腺中rag1表达显著降低。由于胸腺发育依赖咽弓,我们根据咽弓的缺陷将这些突变分为三类。第1类突变体的咽弓没有或仅有轻微形态异常,这意味着这些突变可能包括淋巴细胞发育和胸腺上皮细胞成熟等胸腺特异性事件中的缺陷。第2类突变体的咽弓形状异常。第3类突变体表现出严重的咽弓发育减弱。在第2类和第3类突变体中,胸腺发育的缺陷可能是由于咽弓发育异常。预计这些突变将有助于确定胸腺器官发生的分子机制。