Jungbluth S, Bell E, Lumsden A
Department of Developmental Neurobiology, King's College London, Hodgkin Building, Guy's Campus, London SE1 9RT, UK.
Development. 1999 Jun;126(12):2751-8. doi: 10.1242/dev.126.12.2751.
Hox genes have been implicated in specifying positional values along the anteroposterior axis of the caudal central nervous system, but their nested and overlapping expression has complicated the understanding of how they confer specific neural identity. We have employed a direct gain-of-function approach using retroviral vectors to misexpress Hoxa2 and Hoxb1 outside of the normal Hox expression domains, thereby avoiding complications resulting from possible interactions with endogenous Hox genes. Misexpression of either Hoxa2 or Hoxb1 in the anteriormost hindbrain (rhombomere1, r1) leads to the generation of motor neurons in this territory, even though it is normally devoid of this cell type. These ectopic neurons have the specific identity of branchiomotor neurons and, in the case of Hoxb1-induced cells, their axons leave the hindbrain either by fasciculating with the resident cranial motor axons at isthmic (trochlear) or r2 (trigeminal) levels of the axis or via novel ectopic exit points in r1. Next, we have attempted to identify the precise branchiomotor subtypes that are generated after misexpression and our results suggest that the ectopic motor neurons generated following Hoxa2 misexpression are trigeminal-like, while those generated following Hoxb1 misexpression are facial-like. Our data demonstrate, therefore, that at least to a certain extent and for certain cell types, the singular activities of individual Hox genes (compared to a combinatorial mode of action, for example) are sufficient to impose on neuronal precursor cells the competence to generate distinctly specified cell types. Moreover, as these particular motor neuron subtypes are normally generated in the most anterior domains of Hoxa2 and Hoxb1 expression, respectively, our data support the idea that the main site of individual Hox gene action is in the anteriormost subdomain of their expression, consistent with the phenomenon of posterior dominance.
Hox基因与尾端中枢神经系统前后轴位置值的确定有关,但其嵌套和重叠表达使人们难以理解它们如何赋予特定的神经身份。我们采用了一种直接的功能获得方法,利用逆转录病毒载体在正常Hox表达域之外错误表达Hoxa2和Hoxb1,从而避免了与内源性Hox基因可能相互作用带来的复杂性。在最前端的后脑(菱脑节1,r1)中错误表达Hoxa2或Hoxb1都会导致该区域产生运动神经元,尽管该区域通常没有这种细胞类型。这些异位神经元具有鳃运动神经元的特定身份,就Hoxb1诱导的细胞而言,它们的轴突通过与轴的峡部(滑车神经)或r2(三叉神经)水平的驻留颅运动轴突成束,或者通过r1中的新异位出口点离开后脑。接下来,我们试图确定错误表达后产生的精确鳃运动神经元亚型,我们的结果表明,Hoxa2错误表达后产生的异位运动神经元类似三叉神经,而Hoxb1错误表达后产生的则类似面神经。因此,我们的数据表明,至少在一定程度上,对于某些细胞类型,单个Hox基因的单一活性(例如,与组合作用模式相比)足以赋予神经元前体细胞产生明确指定细胞类型的能力。此外,由于这些特定的运动神经元亚型通常分别在Hoxa2和Hoxb1表达的最前端区域产生,我们的数据支持这样一种观点,即单个Hox基因作用的主要位点在其表达的最前端子域,这与后优势现象一致。