spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hoshizaki, D. K.
Right arrow Articles by Sweis, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hoshizaki, D. K.
Right arrow Articles by Sweis, R.

Development, Vol 120, Issue 9 2489-2499, Copyright © 1994 by Company of Biologists


JOURNAL ARTICLES

Embryonic fat-cell lineage in Drosophila melanogaster

DK Hoshizaki, T Blackburn, C Price, M Ghosh, K Miles, M Ragucci and R Sweis
Department of Biochemistry, University of Illinois, College of Medicine at Chicago 60612.

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)


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
Z. Xu, S. Yu, C.-H. Hsu, J. Eguchi, and E. D. Rosen
The orphan nuclear receptor chicken ovalbumin upstream promoter-transcription factor II is a critical regulator of adipogenesis
PNAS, February 19, 2008; 105(7): 2421 - 2426.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. A. Myers, S.-C. M. Wang, and G. E. O. Muscat
The Chicken Ovalbumin Upstream Promoter-Transcription Factors Modulate Genes and Pathways Involved in Skeletal Muscle Cell Metabolism
J. Biol. Chem., August 25, 2006; 281(34): 24149 - 24160.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. G. Smith and G. E. O. Muscat
Orphan nuclear receptors: therapeutic opportunities in skeletal muscle
Am J Physiol Cell Physiol, August 1, 2006; 291(2): C203 - C217.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
M. Fu, T. Sun, A. L. Bookout, M. Downes, R. T. Yu, R. M. Evans, and D. J. Mangelsdorf
A Nuclear Receptor Atlas: 3T3-L1 Adipogenesis
Mol. Endocrinol., October 1, 2005; 19(10): 2437 - 2450.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
P. M. Domingos, M. Mlodzik, C. S. Mendes, S. Brown, H. Steller, and B. Mollereau
Spalt transcription factors are required for R3/R4 specification and establishment of planar cell polarity in the Drosophila eye
Development, November 15, 2004; 131(22): 5695 - 5702.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Hayes, J. Miller, and D. Hoshizaki
serpent, a GATA-like transcription factor gene, induces fat-cell development in Drosophila melanogaster
Development, January 4, 2001; 128(7): 1193 - 1200.
[Abstract] [PDF]


Home page
Mol. Endocrinol.Home page
F. Adam, T. Sourisseau, R. Métivier, Y. Le Page, C. Desbois, D. Michel, and G. Salbert
COUP-TFI (Chicken Ovalbumin Upstream Promoter-Transcription Factor I) Regulates Cell Migration and Axogenesis in Differentiating P19 Embryonal Carcinoma Cells
Mol. Endocrinol., December 1, 2000; 14(12): 1918 - 1933.
[Abstract] [Full Text]


Home page
DevelopmentHome page
L. Moore, H. Broihier, M Van Doren, and R Lehmann
Gonadal mesoderm and fat body initially follow a common developmental path in Drosophila
Development, January 3, 1998; 125(5): 837 - 844.
[Abstract] [PDF]


Home page
DevelopmentHome page
V Riechmann, K. Rehorn, R Reuter, and M Leptin
The genetic control of the distinction between fat body and gonadal mesoderm in Drosophila
Development, January 2, 1998; 125(4): 713 - 723.
[Abstract] [PDF]


Home page
Endocr. Rev.Home page
S. Y. Tsai and M.-J. Tsai
Chick Ovalbumin Upstream Promoter-Transcription Factors (COUP-TFs): Coming of Age
Endocr. Rev., April 1, 1997; 18(2): 229 - 240.
[Abstract] [Full Text]


Home page
DevelopmentHome page
S. Lin, M. Lin, P Horvath, K. Reddy, and R. Storti
PDP1, a novel Drosophila PAR domain bZIP transcription factor expressed in developing mesoderm, endoderm and ectoderm, is a transcriptional regulator of somatic muscle genes
Development, January 11, 1997; 124(22): 4685 - 4696.
[Abstract] [PDF]


Home page
Genes Dev.Home page
N Azpiazu, P A Lawrence, J P Vincent, and M Frasch
Segmentation and specification of the Drosophila mesoderm.
Genes & Dev., December 15, 1996; 10(24): 3183 - 3194.
[Abstract] [PDF]


Home page
Genes Dev.Home page
M Beiman, B Z Shilo, and T Volk
Heartless, a Drosophila FGF receptor homolog, is essential for cell migration and establishment of several mesodermal lineages.
Genes & Dev., December 1, 1996; 10(23): 2993 - 3002.
[Abstract] [PDF]


Home page
DevelopmentHome page
K. Rehorn, H Thelen, A. Michelson, and R Reuter
A molecular aspect of hematopoiesis and endoderm development common to vertebrates and Drosophila
Development, January 12, 1996; 122(12): 4023 - 4031.
[Abstract] [PDF]


Home page
DevelopmentHome page
J Broadus and C. Doe
Evolution of neuroblast identity: seven-up and prospero expression reveal homologous and divergent neuroblast fates in Drosophila and Schistocerca
Development, January 12, 1995; 121(12): 3989 - 3996.
[Abstract] [PDF]


Home page
DevelopmentHome page
O. Borkowski, N. Brown, and M Bate
Anterior-posterior subdivision and the diversification of the mesoderm in Drosophila
Development, January 12, 1995; 121(12): 4183 - 4193.
[Abstract] [PDF]


Home page
DevelopmentHome page
S Kramer, S. West, and Y Hiromi
Cell fate control in the Drosophila retina by the orphan receptor seven-up: its role in the decisions mediated by the ras signaling pathway
Development, January 5, 1995; 121(5): 1361 - 1372.
[Abstract] [PDF]




© The Company of Biologists Ltd 1994