Differential screening of a PCR-generated mouse embryo cDNA library: glucose transporters are differentially expressed in early postimplantation mouse embryos
Open Access
- 1 November 1992
- journal article
- Published by The Company of Biologists in Development
- Vol. 116 (3) , 555-561
- https://doi.org/10.1242/dev.116.3.555
Abstract
Differential screening of a cDNA library constructed using PCR amplification techniques from RNA isolated from the distal portion (embryonic ectoderm, mesoderm and visceral endoderm) of 7.5 days post coitum (dpc) mouse embryos led to the isolation of two cDNA clones expressed at higher levels in 7.5 dpc embryos than 12.5 dpc embryos. Nucleotide sequence analysis revealed that each of these clones was a different member of the family of facilitative glucose transporters (Glut genes). The differentially expressed cDNA clones represent mouse Glut-1 and Glut-3. Levels of the Glut-3 mRNA declined 14-fold between days 7.5 and 12.5 of gestation, and were under our limits of detetction by 14.5 dpc. The levels of the Glut-1 mRNA declined about 3-fold between days 7.5 and 12.5 of gestation. Analysis of the expression of these genes by in situ hybridization revealed striking differences in transcript localization in early postimplantation mouse embryos. At 7.5 dpc, both transporters were expressed more strongly in extraembryonic tissues than in the embryo proper. While both transporters were expressed in the amnion and chorion, only Glut-1 was expressed in the ectoplacental cone. In the yolk sac, Glut-3 appeared to be expressed only in the endoderm while Glut-1, although expressed in both layers, was expressed more strongly in the mesoderm layer. Thus, the two transporters have relatively reciprocal sites of expression in the developing extraembryonic membranes. Expression of Glut-1 was fairly widespread in the embryo at 8.5 dpc, but by 10.5 dpc expression was down-regulated and was observed in the eye and the spinal cord. Expression of Glut-3 was largely confined to non-neural surface ectoderm and was also substantially down-regulated by 10.5 dpc. These results prompted an examination of the RNA expression pattern of two other glucose transporter isoforms, Glut-2 and Glut-4. We did not detect Glut-4 expression, while Glut-2 expression was largely confined to extraembryonic visceral yolk sac endoderm. These data suggest differential roles for these glucose transporter family members during early postimplantation development of mice.Keywords
This publication has 28 references indexed in Scilit:
- Mammalian Facilitative Glucose Transporter Family: Structure and Molecular RegulationAnnual Review of Physiology, 1992
- STRUCTURE AND FUNCTION OF HEXOSE TRANSPORTERSAnnual Review of Biochemistry, 1991
- Expression of multiple novel Wnt-1/int-1-related genes during fetal and adult mouse development.Genes & Development, 1990
- Murine Developmental Control GenesScience, 1990
- 3T3-L1 Adipocyte glucose transporter (HepG2 Class): Sequence and regulation of protein and mRNA expression by insulin, differentiation, and glucose starvationArchives of Biochemistry and Biophysics, 1990
- Cloning of PCR-amplified total cDNA: Construction of a mouse oocyte cDNA libraryGene Analysis Techniques, 1990
- Family of Glucose-Transporter Genes: Implications for Glucose Homeostasis and DiabetesDiabetes, 1990
- Cloning and functional expression in bacteria of a novel glucose transporter present in liver, intestine, kidney, and β-pancreatic islet cellsCell, 1988
- Effects of maternal diabetes on early embryogenesis: II. Hyperglycemia-induced exencephalyTeratology, 1980
- Teratogenic effects of excess glucose on head‐fold rat embryos in cultureTeratology, 1977