Sasado Takao, Morinaga Chikako, Niwa Katsutoshi, Shinomiya Ai, Yasuoka Akihito, Suwa Hiroshi, Hirose Yukihiro, Yoda Hiroki, Henrich Thorsten, Deguchi Tomonori, Iwanami Norimasa, Watanabe Tomomi, Kunimatsu Sanae, Osakada Masakazu, Okamoto Yasuko, Kota Yasuko, Yamanaka Toshiyuki, Tanaka Minoru, Kondoh Hisato, Furutani-Seiki Makoto
Japan Science and Technology Agency, ERATO Kondoh Differentiation Signaling Project, Kondoh Research Group, Kinki-chihou Hatsumei Center Building, Yoshida-Kawaramachi 14, Sakyo-ku, Kyoto 606-8305, Japan.
Mech Dev. 2004 Jul;121(7-8):817-28. doi: 10.1016/j.mod.2004.03.022.
The development of germ cells has been intensively studied in Medaka (Oryzias latipes). We have undertaken a large-scale screen to identify mutations affecting the development of primordial germ cells (PGCs) in Medaka. Embryos derived from mutagenized founder fish were screened for an abnormal distribution or number of PGCs at embryonic stage 27 by RNA in situ hybridization for the Medaka vasa homologue (olvas). At this stage, PGCs coalesce into two bilateral vasa-expressing foci in the ventrolateral regions of the trunk after their migration and group organization. Nineteen mutations were identified from a screen corresponding to 450 mutagenized haploid genomes. Eleven of the mutations caused altered PGC distribution. Most of these alterations were associated with morphological abnormalities and could be grouped into four phenotypic classes: Class 1, PGCs dispersed into bilateral lines; Class 2, PGCs dispersed in a region more medial than that in Class 1; Class 3, PGCs scattered laterally and over the yolk sac area; and Class 4, PGCs clustered in a single median focus. Eight mutations caused a decrease in the number of PGCs. This decrease was observed in the offspring of heterozygous mothers, indicating the contribution of a maternal factor in determining PGC abundance. Taken together, these mutations should prove useful in identifying molecular mechanisms underlying the early PGC development and migration.
在青鳉(日本青鳉)中,生殖细胞的发育已经得到了深入研究。我们进行了一项大规模筛选,以鉴定影响青鳉原始生殖细胞(PGC)发育的突变。通过对青鳉vasa同源物(olvas)进行RNA原位杂交,在胚胎第27阶段筛选来自诱变奠基鱼的胚胎,以检测PGC的分布异常或数量异常。在此阶段,PGC迁移并聚集后,在躯干腹外侧区域合并形成两个表达vasa的双侧病灶。从对应于450个诱变单倍体基因组的筛选中鉴定出19个突变。其中11个突变导致PGC分布改变。这些改变大多与形态异常有关,可分为四个表型类别:第1类,PGC分散成双侧线;第2类,PGC分散在比第1类更内侧的区域;第3类,PGC侧向分散并覆盖卵黄囊区域;第4类,PGC聚集在单个中位点。8个突变导致PGC数量减少。这种减少在杂合子母亲的后代中观察到,表明母体因素在决定PGC丰度方面的作用。综上所述,这些突变应该有助于识别PGC早期发育和迁移背后的分子机制。