Department Biology, Developmental Biology Unit, Erlangen University, Erlangen, Germany.
Dev Biol. 2012 Apr 15;364(2):224-35. doi: 10.1016/j.ydbio.2012.01.024. Epub 2012 Feb 4.
Abdominal patterning in Drosophila requires the function of Nanos (nos) and Pumilio (pum) to repress posterior translation of hunchback mRNA. Here we provide the first functional analysis of nanos and pumilio genes during blastodermal patterning of a short-germ insect. We found that nos and pum in the red flour beetle Tribolium castaneum crucially contribute to posterior segmentation by preventing hunchback translation. While this function seems to be conserved among insects, we provide evidence that Nos and Pum may also act on giant expression, another gap gene. After depletion of nos and pum by parental RNAi, Hunchback and giant remain ectopically at the posterior blastoderm and the posterior Krüppel (Kr) domain is not being activated. giant may be a direct target of Nanos and Pumilio in Tribolium and presumably prevents early Kr expression. In the absence of Kr, the majority of secondary gap gene domains fail to be activated, and abdominal segmentation is terminated prematurely. Surprisingly, we found Nos and Pum also to be involved in early head patterning, as the loss of Nos and Pum results in deletions and transformations of gnathal and pre-gnathal anlagen. Since the targets of Nos and Pum in head development remain to be identified, we propose that anterior patterning in Tribolium may involve additional maternal factors.
在果蝇中,腹部模式的形成需要 Nanos(nos)和 Pumilio(pum)的功能来抑制 hunchback mRNA 的后翻译。在这里,我们首次对短胚昆虫的囊胚模式形成过程中 nanos 和 pumilio 基因进行了功能分析。我们发现,红粉甲虫 Tribolium castaneum 中的 nos 和 pum 对于通过防止 hunchback 翻译来进行后部分化至关重要。虽然这个功能似乎在昆虫中是保守的,但我们提供的证据表明,Nos 和 Pum 也可能作用于 giant 表达,另一个缺口基因。在母体 RNAi 耗尽 nos 和 pum 后,Hunchback 和 giant 仍然在囊胚的后部分异位,并且后 Krüppel(Kr)域未被激活。giant 可能是 Tribolium 中 Nanos 和 Pumilio 的直接靶标,并且可能防止早期 Kr 表达。在没有 Kr 的情况下,大多数次级缺口基因域未能被激活,并且腹部分节过早终止。令人惊讶的是,我们发现 Nos 和 Pum 也参与早期头部模式形成,因为 Nos 和 Pum 的缺失导致 gnathal 和 pre-gnathal 原基的缺失和转化。由于在头部发育中 Nos 和 Pum 的靶标仍有待确定,我们提出 Tribolium 中的前部分化可能涉及其他母体因子。