Ethylnitrosourea-induced thymus-defective mutants identify roles of KIAA1440, TRRAP, and SKIV2L2 in teleost organ development

The thymus is an organ where T lymphocytes develop. Thymus development requires interactions of cells derived from three germ layers. However, the molecular mechanisms that control thymus development are not fully understood. To identify the genes that regulate thymus development, we previously carr...

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Veröffentlicht in:European journal of immunology 2009-09, Vol.39 (9), p.2606-2616
Hauptverfasser: Iwanami, Norimasa, Okada, Minoru, Hoa, Vu Q, Seo, Yasuhito, Mitani, Hiroshi, Sasaki, Takashi, Shimizu, Nobuyoshi, Kondoh, Hisato, Furutani-Seiki, Makoto, Takahama, Yousuke
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container_end_page 2616
container_issue 9
container_start_page 2606
container_title European journal of immunology
container_volume 39
creator Iwanami, Norimasa
Okada, Minoru
Hoa, Vu Q
Seo, Yasuhito
Mitani, Hiroshi
Sasaki, Takashi
Shimizu, Nobuyoshi
Kondoh, Hisato
Furutani-Seiki, Makoto
Takahama, Yousuke
description The thymus is an organ where T lymphocytes develop. Thymus development requires interactions of cells derived from three germ layers. However, the molecular mechanisms that control thymus development are not fully understood. To identify the genes that regulate thymus development, we previously carried out a large-scale screening for ethylnitrosourea-induced mutagenesis using medaka, Oryzias latipes, and established a panel of recessive thymus-lacking mutants. Here we report the identification of three genes responsible for these mutations. We found that the mutations in KIAA1440, TRRAP, and SKIV2L2 caused the defects in distinct steps of thymus development. We also found that these genes were widely expressed in many organs and that the mutations in these genes caused defects in the development of various other organs. These results enabled us to identify previously unknown roles of widely expressed genes in medaka organ development. The possible reasons why thymus-defective teleost mutants could be used to identify widely expressed genes and future strategies to increase the likelihood of identifying genes that specifically regulate thymus development are discussed.
doi_str_mv 10.1002/eji.200939362
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Thymus development requires interactions of cells derived from three germ layers. However, the molecular mechanisms that control thymus development are not fully understood. To identify the genes that regulate thymus development, we previously carried out a large-scale screening for ethylnitrosourea-induced mutagenesis using medaka, Oryzias latipes, and established a panel of recessive thymus-lacking mutants. Here we report the identification of three genes responsible for these mutations. We found that the mutations in KIAA1440, TRRAP, and SKIV2L2 caused the defects in distinct steps of thymus development. We also found that these genes were widely expressed in many organs and that the mutations in these genes caused defects in the development of various other organs. These results enabled us to identify previously unknown roles of widely expressed genes in medaka organ development. 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subjects Adaptor Proteins, Signal Transducing - genetics
Adaptor Proteins, Signal Transducing - physiology
Alternative Splicing
Animals
Base Sequence
Ethylnitrosourea - pharmacology
Ethylnitrosourea‐induced mutagenesis
Exons - genetics
Medaka
Molecular Sequence Data
Mutation
Nuclear Proteins - genetics
Nuclear Proteins - physiology
Organogenesis
Organogenesis - genetics
Oryzias - embryology
Oryzias - genetics
Oryzias - immunology
Positional cloning
RNA Helicases - genetics
RNA Helicases - physiology
Thymus
Thymus Gland - embryology
title Ethylnitrosourea-induced thymus-defective mutants identify roles of KIAA1440, TRRAP, and SKIV2L2 in teleost organ development
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