Yasuoka Akihito, Hirose Yukihiro, Yoda Hiroki, Aihara Yoshiko, Suwa Hiroshi, Niwa Katsutoshi, Sasado Takao, Morinaga Chikako, Deguchi Tomonori, Henrich Thorsten, Iwanami Norimasa, Kunimatsu Sanae, Abe Keiko, Kondoh Hisato, Furutani-Seiki Makoto
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.
Mech Dev. 2004 Jul;121(7-8):729-38. doi: 10.1016/j.mod.2004.03.032.
We performed a systematic screen for mutations affecting the trajectory of axons visualized by immunohistochemical staining of Medaka embryos with anti-acetylated tubulin antibody. Among the mutations identified, yanagi (yan) and kazura (kaz) mutations caused specific defects in projection of the posterior lateral line (PLL) nerve. In yan and kaz mutant embryos, the PLL nerve main bundle was misrouted ventrally and dorsally or anteriorly. Medaka semaphorin3A, sdf1, and cxcr4 cDNA fragments were cloned to allow analysis of these mutants. There were no changes in semaphorin3A or sdf1 expression in mutant embryos, suggesting that the tissues expressing semaphorin3A or sdf1 that are involved in PLL nerve guidance are present in these mutant embryos. Double staining revealed that the mislocated PLL primordium and growth cone of the ectopically projected PLL nerve were always colocalized in both yan and kaz mutant embryos, suggesting that migration of PLL primordia and PLL nerve growth cones are not uncoupled in these mutants. Although homozygous yan larvae showed incomplete migration of the PLL primordium along the anteroposterior axis, ventral proneuromast migration was complete, suggesting that ventral migration of the proneuromast does not require the signaling affected in yan mutants. In addition to the PLL system, the distribution of primordial germ cells (PGCs) was also affected in both yan and kaz mutant embryos, indicating that yan and kaz genes are required for the migration of both PLL primordia and PGCs. Genetic linkage analysis indicated that kaz is linked to cxcr4, but yan is not linked to sdf1 or cxcr4. These mutations will provide genetic clues to investigate the molecular mechanism underlying formation of the PLL system.
我们通过用抗乙酰化微管蛋白抗体对青鳉胚胎进行免疫组织化学染色,对影响轴突轨迹的突变进行了系统筛选。在鉴定出的突变中,柳(yan)和葛(kaz)突变导致后侧线(PLL)神经投射出现特定缺陷。在yan和kaz突变胚胎中,PLL神经主束向腹侧、背侧或前方误布线。克隆了青鳉信号素3A、sdf1和cxcr4 cDNA片段,以便对这些突变体进行分析。突变胚胎中信号素3A或sdf1的表达没有变化,这表明参与PLL神经导向的表达信号素3A或sdf1的组织在这些突变胚胎中存在。双重染色显示,异位投射的PLL神经的错位PLL原基和生长锥在yan和kaz突变胚胎中总是共定位的,这表明在这些突变体中PLL原基和PLL神经生长锥的迁移并非解偶联。虽然纯合的yan幼虫显示PLL原基沿前后轴的迁移不完全,但腹侧原神经丘的迁移是完全的,这表明原神经丘的腹侧迁移不需要yan突变体中受影响的信号传导。除了PLL系统外,yan和kaz突变胚胎中原始生殖细胞(PGC)的分布也受到影响,这表明yan和kaz基因是PLL原基和PGC迁移所必需的。遗传连锁分析表明,kaz与cxcr4连锁,但yan与sdf1或cxcr4不连锁。这些突变将为研究PLL系统形成的分子机制提供遗传线索。