首页> 外文期刊>Developmental genetics >EFFECTS OF ALL-TRANS-RETINOIC ACID ON SKELETAL PATTERN, 5'HOXD GENE EXPRESSION, AND RAR-BETA-2/BETA-4 PROMOTER ACTIVITY IN EMBRYONIC MOUSE LIMBS
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EFFECTS OF ALL-TRANS-RETINOIC ACID ON SKELETAL PATTERN, 5'HOXD GENE EXPRESSION, AND RAR-BETA-2/BETA-4 PROMOTER ACTIVITY IN EMBRYONIC MOUSE LIMBS

机译:全反式维甲酸对胚胎小鼠肢体骨骼肌形态,5'HOXD基因表达及RAR-BETA-2 / BETA-4启动子活性的影响

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Mouse embryos were exposed to all-trans-retinoic acid on day 11 or day 12 of development and the resulting skeletal pattern alterations compared with early effects on Hoxd-11 and Hoxd-13 expression domains and RAR-beta 2/beta 4 promoter activity. The effects on skeletal pattern showed a clear correlation between the timing of retinoic acid exposure and the sequence of mesenchymal condensation. Ectopic RAR-beta 2/beta 4 promoter activity was detected within 2 hr of exposure to retinoic acid, and was present throughout the limb bud after 5 hr; it remained high in the apical ectodermal ridge and proximal mesenchyme after 12 hr, by which time the abnormal digital pattern could be seen. HoxD gene expression domains in the distal handplate were narrowed by 5 hr after maternal retinoic acid administration on day 11. Following retinoic acid treatment on both day 11 and day 12, the normal downregulation of Hoxd-11 and Hoxd-13 in the digital mesenchymal condensations was retarded. There was no evidence to suggest that RAR-beta 2/beta 4 promoter activity mediates the effects of RA on HoxD gene expression, but ectopic promoter activity is a useful indicator of at least some of the sites in which RA levels are raised. We suggest (1) that the apical ectodermal ridge is the most functionally significant of these sites, (2) that raised retinoic acid levels in the ridge result in altered gene expression and/or altered cell proliferation within this epithelium, (3) that both altered HoxD ene expression domains and altered skeletal pattern formation are secondary to this effect. There was a good correlation between the effects of retinoic acid on Hoxd-11 and Hoxd-13 expression and delay of skeletal differentiation, suggesting that this may be a direct effect.
机译:小鼠胚胎在发育的第11天或第12天暴露于全反式维甲酸,与早期对Hoxd-11和Hoxd-13表达域以及RAR-beta 2 / beta 4启动子活性的影响相比,骨骼结构发生了变化。对骨骼形态的影响表明,视黄酸的暴露时间与间充质凝结的顺序之间存在明显的相关性。在暴露于视黄酸的2小时内检测到异位RAR-beta 2 / beta 4启动子活性,并在5小时后遍及整个肢芽。 12小时后,其在根尖外胚层脊和近端间充质中仍保持较高水平,此时可以看到异常的数字模式。在第11天给予母体视黄酸后5小时,将远端手板中的HoxD基因表达域缩小5小时。在第11天和第12天进行视黄酸治疗后,数字间充质中Hoxd-11和Hoxd-13正常下调。智障。没有证据表明RAR-beta 2 / beta 4启动子活性介导了RA对HoxD基因表达的影响,但是异位启动子活性是至少某些RA水平升高的有用指标。我们建议(1)顶端外胚层在这些部位中功能最重要;(2)raised中维甲酸水平升高会导致该上皮内的基因表达改变和/或细胞增殖改变;(3)改变的HoxD烯表达域和改变的骨骼模式形成是这种作用的继发因素。视黄酸对Hoxd-11和Hoxd-13表达的影响与骨骼分化延迟之间存在良好的相关性,表明这可能是直接的作用。

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