Laboratory for Genetics and Development, Department of Entomology/Institute of Biotechnology, College of Bio-Resources and Agriculture, National Taiwan University, Taipei, Taiwan.
Insect Mol Biol. 2013 Aug;22(4):442-55. doi: 10.1111/imb.12035. Epub 2013 May 20.
Previously we identified anterior localization of hunchback (Aphb) mRNA in oocytes and early embryos of the parthenogenetic and viviparous pea aphid Acyrthosiphon pisum, suggesting that the breaking of anterior asymmetry in the oocytes leads to the formation of the anterior axis in embryos. In order to study posterior development in the asexual pea aphid, we cloned and analysed the developmental expression of caudal (Apcad), a posterior gene highly conserved in many animal phyla. We found that transcripts of Apcad were not detected in germaria, oocytes and embryos prior to the formation of the blastoderm in the asexual (viviparous) pea aphid. This unusual expression pattern differs from that of the existing insect models, including long- and short-germ insects, where maternal cad mRNA is passed to the early embryos and forms a posterior-anterior gradient. The first detectable Apcad expression occurred in the newly formed primordial germ cells and their adjacent blastodermal cells during late blastulation. From gastrulation onward, and as in other insects, Apcad mRNA is restricted to the posteriormost region of the germ band. Similarly, in the sexual (oviparous) oocytes we were able to identify anterior localization of Aphb mRNA but posterior localization of Apcad was not detected. This suggests that cad-driven posterior development is not conserved during early embryogenesis in asexual and sexual pea aphids.
先前,我们发现豌豆蚜孤雌生殖和胎生的卵母细胞和早期胚胎中 hunchback(Aphb)mRNA 定位于前端,这表明卵母细胞前端不对称的破坏导致胚胎前端轴的形成。为了研究无性豌豆蚜的后端发育,我们克隆并分析了高度保守于许多动物门的后端基因 caudal(Apcad)的发育表达。我们发现,在无性(胎生)豌豆蚜的胚盘形成之前,Apcad 的转录本在生殖腺、卵母细胞和胚胎中无法检测到。这种不寻常的表达模式与现有的昆虫模型不同,包括长胚和短胚昆虫,其中母体 cad mRNA 传递到早期胚胎并形成后端-前端梯度。在晚期原肠胚形成期间,第一个可检测到的 Apcad 表达发生在新形成的原始生殖细胞及其相邻的胚盘细胞中。从原肠胚形成开始,与其他昆虫一样,Apcad mRNA 局限于生殖带的后极区域。同样,在有性(卵生)卵母细胞中,我们能够鉴定 Aphb mRNA 的前端定位,但未检测到 Apcad 的后端定位。这表明 cad 驱动的后端发育在无性和有性豌豆蚜的早期胚胎发生中没有保守。