Linnemannstöns Karen, Ripp Caroline, Honemann-Capito Mona, Brechtel-Curth Katja, Hedderich Marie, Wodarz Andreas
Stem Cell Biology, Institute for Anatomy and Cell Biology, University of Goettingen, Goettingen, Germany.
Institute for Developmental Biochemistry, University of Goettingen, Goettingen, Germany.
PLoS Genet. 2014 Jul 10;10(7):e1004443. doi: 10.1371/journal.pgen.1004443. eCollection 2014 Jul.
Wnt proteins regulate many developmental processes and are required for tissue homeostasis in adult animals. The cellular responses to Wnts are manifold and are determined by the respective Wnt ligand and its specific receptor complex in the plasma membrane. Wnt receptor complexes contain a member of the Frizzled family of serpentine receptors and a co-receptor, which commonly is a single-pass transmembrane protein. Vertebrate protein tyrosine kinase 7 (PTK7) was identified as a Wnt co-receptor required for control of planar cell polarity (PCP) in frogs and mice. We found that flies homozygous for a complete knock-out of the Drosophila PTK7 homolog off track (otk) are viable and fertile and do not show PCP phenotypes. We discovered an otk paralog (otk2, CG8964), which is co-expressed with otk throughout embryonic and larval development. Otk and Otk2 bind to each other and form complexes with Frizzled, Frizzled2 and Wnt2, pointing to a function as Wnt co-receptors. Flies lacking both otk and otk2 are viable but male sterile due to defective morphogenesis of the ejaculatory duct. Overexpression of Otk causes female sterility due to malformation of the oviduct, indicating that Otk and Otk2 are specifically involved in the sexually dimorphic development of the genital tract.
Wnt蛋白调控许多发育过程,并且是成年动物组织稳态所必需的。细胞对Wnt的反应多种多样,并且由各自的Wnt配体及其在质膜中的特异性受体复合物决定。Wnt受体复合物包含一个卷曲蛋白家族的蛇形受体成员和一个共受体,该共受体通常是单次跨膜蛋白。脊椎动物蛋白酪氨酸激酶7(PTK7)被鉴定为青蛙和小鼠中控制平面细胞极性(PCP)所需的Wnt共受体。我们发现,果蝇PTK7同源物偏离轨道(otk)完全敲除的纯合子果蝇是有活力且可育的,并且不表现出PCP表型。我们发现了一个otk旁系同源物(otk2,CG8964),它在整个胚胎和幼虫发育过程中与otk共表达。Otk和Otk2相互结合,并与卷曲蛋白、卷曲蛋白2和Wnt2形成复合物,表明其具有Wnt共受体的功能。同时缺乏otk和otk2的果蝇是有活力的,但由于射精管形态发生缺陷而雄性不育。Otk的过表达由于输卵管畸形导致雌性不育,这表明Otk和Otk2特别参与生殖道的性别二态性发育。