Hanaoka Ryuki, Dawid Igor B, Kawahara Atsuo
Laboratory of Developmental Molecular Genetics, Graduate School of Medicine, Kyoto University, Yoshida Konoe-cho, Sakyo-Ku, Kyoto, Japan.
DNA Seq. 2007 Feb;18(1):54-60. doi: 10.1080/10425170601060848.
Heme is synthesized from glycine and succinyl CoA by eight heme synthesis enzymes. Although genetic defects in any of these enzymes are known to cause severe human blood diseases, their developmental expression in mammals is unknown. In this paper, we report two zebrafish heme synthesis enzymes, uroporphyrinogen III synthase (UROS) and protoporphyrinogen oxidase (PPO) that are well conserved in comparison to their human counterparts. Both UROS and PPO formed pairs of bilateral stripes in the lateral plate mesoderm at the 15-somite stage. At 24 h post-fertilization (hpf), UROS and PPO were predominantly expressed in the intermediate cell mass (ICM) that is the major site of primitive hematopoiesis. The expression of UROS and PPO was drastically suppressed in the bloodless mutants cloche and vlad tepes/gata 1 from 15-somite to 24hpf stages, indicating that both cloche and vlad tepes/gata 1 are required for the induction and maintenance of UROS and PPO expression in the ICM.
血红素由八种血红素合成酶从甘氨酸和琥珀酰辅酶A合成。虽然已知这些酶中的任何一种发生基因缺陷都会导致严重的人类血液疾病,但它们在哺乳动物中的发育表达情况尚不清楚。在本文中,我们报告了两种斑马鱼血红素合成酶,即尿卟啉原III合成酶(UROS)和原卟啉原氧化酶(PPO),与它们的人类对应物相比,它们具有高度保守性。在15体节期,UROS和PPO在侧板中胚层形成双侧条纹对。在受精后24小时(hpf),UROS和PPO主要在原始造血的主要部位中间细胞群(ICM)中表达。在15体节到24hpf阶段,无血突变体cloche和vlad tepes/gata 1中UROS和PPO的表达被显著抑制,这表明cloche和vlad tepes/gata 1对于ICM中UROS和PPO表达的诱导和维持都是必需的。