Hoshizaki D K, Blackburn T, Price C, Ghosh M, Miles K, Ragucci M, Sweis R
Department of Biochemistry, University of Illinois, College of Medicine at Chicago 60612.
Development. 1994 Sep;120(9):2489-99. doi: 10.1242/dev.120.9.2489.
The Drosophila adipose tissue, or fat body, and the bodywall muscle are two major tissues derived from the mesoderm. Although much is known about the lineage of muscle cells, little is known about the development of the fat body. Using known genes and an enhancer trap (29D), we have begun to trace the lineage of the cells comprising the fat body. The genes Adh (alcohol dehydrogenase) and DCg1 (type IV collagen) code for gene products involved in fat-cell metabolism and therefore serve as terminal fat-cell differentiation markers. The expression of these genes was used to identify the fat body at stage 17 and to identify the start of terminal fat-cell differentiation at stage 15. We found that the steroid-hormone receptor gene, svp (seven-up), was expressed transiently within the fat-cell lineage from stages 12 to 14. We suggest that stage 12 marks the beginning of early fat-cell differentiation and that the svp-positive cells within the mesoderm are early precursor fat cells. To confirm the identity of these cells and to establish the role of svp in the developing fat cell, we examined svp mutant embryos for alterations in the expression of the two terminal fat-cell differentiation markers, Adh and DCg1. Loss of svp function resulted in the loss of Adh transcript and a reduction of DCg1 expression specifically in the fat body. Thus, svp plays a role in fat-body-specific expression of at least two terminal fat-cell differentiation genes. In contrast to svp, we found no evidence that the steroid receptor HNF-4(D) gene was expressed in the fat body nor that it was involved in the development of this tissue. Using an enhancer-trap line (29D), we further traced the fat-cell lineage to nine bilateral clusters of cells within the mesoderm at germ-band extension. We suggest these 29D-positive cells represent the progenitor fat cells. In stage-12 embryos, the 29D-positive cell clusters can be identified within the mesoderm internal to nautilus-expressing cells. These data suggest that the precursor fat cells may be derived from the inner mesoderm, or spanchnopleura. Embryos deficient for the DNA region surrounding the site of the 29D enhancer trap lack most, if not all, of the cells in the fat-cell lineage. These embryos exhibit the loss of svp-positive precursor fat cells and concomitant loss of fat-body-specific expression of Adh and DCg1.(ABSTRACT TRUNCATED AT 400 WORDS)
果蝇的脂肪组织,即脂肪体,以及体壁肌肉是源自中胚层的两种主要组织。尽管人们对肌肉细胞的谱系了解很多,但对脂肪体的发育却知之甚少。利用已知基因和一个增强子陷阱(29D),我们已开始追踪构成脂肪体的细胞谱系。基因Adh(乙醇脱氢酶)和DCg1(IV型胶原蛋白)编码参与脂肪细胞代谢的基因产物,因此可作为脂肪细胞终末分化的标志物。这些基因的表达被用于在17期鉴定脂肪体,并在15期鉴定脂肪细胞终末分化的起始。我们发现,类固醇激素受体基因svp(七上)在12至14期在脂肪细胞谱系中短暂表达。我们认为12期标志着早期脂肪细胞分化的开始,中胚层内svp阳性细胞是早期脂肪前体细胞。为了确认这些细胞的身份并确定svp在发育中的脂肪细胞中的作用,我们检查了svp突变胚胎中两种脂肪细胞终末分化标志物Adh和DCg1表达的变化。svp功能丧失导致Adh转录本缺失,且DCg1表达在脂肪体中特异性降低。因此,svp在至少两种脂肪细胞终末分化基因的脂肪体特异性表达中发挥作用。与svp不同,我们没有发现类固醇受体HNF-4(D)基因在脂肪体中表达或参与该组织发育的证据。利用一个增强子陷阱品系(29D),我们进一步将脂肪细胞谱系追溯到胚带延伸时中胚层内的九个双侧细胞簇。我们认为这些29D阳性细胞代表脂肪前体细胞。在12期胚胎中,可在表达鹦鹉螺蛋白的细胞内部的中胚层内鉴定出29D阳性细胞簇。这些数据表明脂肪前体细胞可能源自内中胚层,即脏壁中胚层。缺乏29D增强子陷阱位点周围DNA区域的胚胎缺乏脂肪细胞谱系中的大部分(如果不是全部)细胞。这些胚胎表现出svp阳性脂肪前体细胞缺失,以及Adh和DCg1脂肪体特异性表达的伴随缺失。(摘要截短于400字)