Hagiuda Jun, Hiraoka Yoshiki, Hasegawa Masanori, Ogawa Motoyuki, Aiso Sadakazu
Department of Anatomy, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo 160-8582, Japan.
Biochim Biophys Acta. 2003 Jul 28;1628(2):140-5. doi: 10.1016/s0167-4781(03)00139-8.
The sex-determining region Y (SRY) gene and its related Sox genes encode transcriptional regulatory factors. In this study, we isolated and sequenced a novel Sox cDNA from African clawed frog (Xenopus laevis). The Sox gene was named xSox33. xSox33 was revealed to encode 244 amino acids. Reverse transcription-polymerase chain reaction (RT-PCR) showed that xSox33 was expressed at very low levels in some frog tissues including lung, ovary, skeletal muscle, testis, brain and heart. Its embryonic expression was also studied by RT-PCR. After the mid-blastula transition, the zygotic expression was initiated during gastrulation and the level was elevated as the embryogenesis proceeded. Electrophoretic mobility shift assay (EMSA) indicated that a recombinant xSox33 polypeptide was capable of binding to the nucleotide sequence AACAAT.
Y染色体性别决定区(SRY)基因及其相关的Sox基因编码转录调节因子。在本研究中,我们从非洲爪蟾(非洲爪蟾)中分离并测序了一个新的Sox cDNA。该Sox基因被命名为xSox33。xSox33被发现编码244个氨基酸。逆转录聚合酶链反应(RT-PCR)表明,xSox33在包括肺、卵巢、骨骼肌、睾丸、脑和心脏在内的一些蛙类组织中表达水平非常低。还通过RT-PCR研究了其胚胎表达。在囊胚中期转变后,合子表达在原肠胚形成期间开始,并且随着胚胎发育的进行水平升高。电泳迁移率变动分析(EMSA)表明,重组xSox33多肽能够与核苷酸序列AACAAT结合。