Isolation and expression of zebrafish zinc-finger transcription factor gene tsh1

被引:4
|
作者
Wang, Han
Lee, Eric Myung-Jae
Sperber, Steven M.
Lin, Shuo
Ekker, Marc
Long, Qiaoming
机构
[1] Univ Ottawa, Dept Biol, Ctr Adv Res Environm Genomics, Ottawa, ON K1N 6N5, Canada
[2] Univ Oklahoma, Dept Zool, Norman, OK 73019 USA
[3] Univ Oklahoma, Stephenson Res & Training Ctr, Norman, OK 73019 USA
[4] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90024 USA
[5] Cornell Univ, Dept Anim Sci, Ithaca, NY 14850 USA
[6] Cornell Univ, Ctr Vertebrate Funct Genomics, Ithaca, NY 14850 USA
关键词
teashirt; transcription factor; neckless; hindbrain; spinal cord; retinoic acid and zebrafish;
D O I
10.1016/j.modgep.2006.08.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report the expression patterns of tsh1, a zebrafish homologue of the Drosophila homeotic gene teashirt. Expression of tsh1 is first detected at the 2-somite stage (10 h post-fertilization, hpf) at the anterior end of the spinal cord. Expression expands toward the posterior spinal cord, and by the prim-5 stage (24 hpf) tsh1 transcripts are detected throughout spinal cord. Between the 14- and 25-somite stage (16-24 hpf), spinal cord expression shows a clear anterior boundary at the rostra] margin of rhombomere 7. Around the prim-25 stage (36 hpf), while the spinal expression of tsh1 decreases, new expression is detected in the pectoral fin buds and dorsal forebrain. By the long-pec stage (48 hpf), spinal cord expression is undetectable, but strong expression is observed in the rhombencephalon, telencephalon, tectum opticum, midbrain-hindbrain boundary, in the first pharyngeal arch and in the eyes. This expression persists at least until the larval stages. Retinoic acid signaling influences tsh1 expression. Zebrafish tsh1 expression was induced in the anterior neural tube in embryos treated briefly with exogenous retinoic acid. Furthermore, tsh1 expression was down-regulated in the spinal cord in the zebrafish neckless mutant in which RA signaling is disrupted due to a missense mutation in the gene encoding retinaldehyde dehydrogenase type 2. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:318 / 322
页数:5
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