Yamada Atsuko, Martindale Mark Q
Kewalo Marine Laboratory, Pacific Biomedical Research Center, University of Hawaii, Honolulu, 96813, USA.
Dev Genes Evol. 2002 Aug;212(7):338-48. doi: 10.1007/s00427-002-0248-x. Epub 2002 Jun 26.
Ctenophores are thoroughly modern animals whose ancestors are derived from a separate evolutionary branch than that of other eumetazoans. Their major longitudinal body axis is the oral-aboral axis. An apical sense organ, called the apical organ, is located at the aboral pole and contains a highly innervated statocyst and photodetecting cells. The apical organ integrates sensory information and controls the locomotory apparatus of ctenophores, the eight longitudinal rows of ctene/comb plates. In an effort to understand the developmental and evolutionary organization of axial properties of ctenophores we have isolated a forkhead gene from the Brain Factor 1 (BF-1) family. This gene, ctenoBF-1, is the first full-length nuclear gene reported from ctenophores. This makes ctenophores the most basal metazoan (to date) known to express definitive forkhead class transcription factors. Orthologs of BF-1 in vertebrates, Drosophila, and Caenorhabditis elegans are expressed in anterior neural structures. Surprisingly, in situ hybridizations with ctenoBF-1 antisense riboprobes show that this gene is not expressed in the apical organ of ctenophores. CtenoBF-1 is expressed prior to first cleavage. Transcripts become localized to the aboral pole by the 8-cell stage and are inherited by ectodermal micromeres generated from this region at the 16- and 32-cell stages. Expression in subsets of these cells persists and is seen around the edge of the blastopore (presumptive mouth) and in distinct ectodermal regions along the tentacular poles. Following gastrulation, stomodeal expression begins to fade and intense staining becomes restricted to two distinct domains in each tentacular feeding apparatus. We suggest that the apical organ is not homologous to the brain of bilaterians but that the oral pole of ctenophores corresponds to the anterior pole of bilaterian animals.
栉水母是完全现代的动物,其祖先源自与其他真后生动物不同的进化分支。它们主要的纵向身体轴是口-反口轴。一个顶端感觉器官,称为顶端器,位于反口极,包含一个高度神经支配的平衡囊和光探测细胞。顶端器整合感觉信息并控制栉水母的运动器官,即八排纵向的栉板。为了理解栉水母轴向特性的发育和进化组织,我们从脑因子1(BF-1)家族中分离出一个叉头基因。这个基因,栉水母BF-1,是从栉水母中报道的第一个全长核基因。这使得栉水母成为已知表达确定的叉头类转录因子的最基础的后生动物(迄今为止)。脊椎动物、果蝇和秀丽隐杆线虫中BF-1的直系同源物在前神经结构中表达。令人惊讶的是,用栉水母BF-1反义核糖探针进行的原位杂交表明,该基因在栉水母的顶端器中不表达。栉水母BF-1在第一次卵裂之前表达。转录本在8细胞阶段定位于反口极,并在16细胞和32细胞阶段由该区域产生的外胚层小细胞继承。这些细胞亚群中的表达持续存在,并在胚孔边缘(推测的口)周围以及沿触手极的不同外胚层区域中可见。原肠胚形成后,口凹表达开始减弱,强烈染色局限于每个触手摄食器官中的两个不同区域。我们认为顶端器与两侧对称动物的脑不同源,但栉水母的口极对应于两侧对称动物的前极。