Gravato-Nobre Maria J, Hodgkin Jonathan
Department of Biochemistry, University of Oxford, Oxford, United Kingdom.
Dev Dyn. 2008 Dec;237(12):3762-76. doi: 10.1002/dvdy.21792.
Susceptibility to the rectal pathogen Microbacterium nematophilum provides a means of examining hindgut differentiation in C. elegans. Mutants of bus-1 are resistant to infection with this pathogen. We show here that bus-1 encodes a predicted acyltransferase expressed in rectal epithelial cells (K, F, and U), suggesting its involvement in regional surface modification. bus-1 reporter genes were used to show spatial regulation by hindgut developmental control genes: egl-38, mab-9, and mab-23. A bus-1::GFP reporter reveals the conspicuous rectal epithelial swelling induced by M. nematophilum. The C. briggsae ortholog of bus-1 exhibits conserved function and rectal expression, but it is expressed in vulval as well as rectal cells, correlated with pathogen adhesion to both vulval and rectal cells in this species. Another acyltransferase affecting bacterial adhesion, bus-18/acl-10, was also identified, which also shows strong rectal expression, but it is expressed in additional epithelial tissues and is required for general surface integrity.
对直肠病原体嗜线虫微杆菌的易感性为研究秀丽隐杆线虫后肠分化提供了一种方法。bus-1突变体对这种病原体的感染具有抗性。我们在此表明,bus-1编码一种预测的酰基转移酶,该酶在直肠上皮细胞(K、F和U)中表达,表明其参与区域表面修饰。bus-1报告基因用于显示后肠发育控制基因egl-38、mab-9和mab-23的空间调控。一个bus-1::GFP报告基因揭示了嗜线虫微杆菌诱导的明显的直肠上皮肿胀。bus-1的秀丽隐杆线虫直系同源物具有保守功能和直肠表达,但它也在外阴细胞以及直肠细胞中表达,这与该物种中外阴和直肠细胞上的病原体粘附相关。还鉴定出了另一种影响细菌粘附的酰基转移酶bus-18/acl-10,它也显示出强烈的直肠表达,但它在其他上皮组织中表达,并且是维持一般表面完整性所必需的。