Perfetti R, Scott L A, Shuldiner A R
Diabetes Unit, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224.
Endocrinology. 1994 Nov;135(5):2037-44. doi: 10.1210/endo.135.5.7956926.
To study the potential role of insulin-like growth factor-I (IGF-I) during early embryogenesis, we have used the amphibian Xenopus laevis, a versatile model of vertebrate development. Using polymerase chain reaction (PCR)-based cloning strategies, we have previously identified two different nonallelic Xenopus IGF-I genes (IGF-I' and IGF-I"). Both are expressed in similar quantities in adult liver. We now report the use of a modification of the reverse transcription-PCR method, designated RNA template-specific PCR (RS-PCR), to detect IGF-I messenger RNA (mRNA) from single oocytes and embryos. The same primer pair was used to amplify both IGF-I' and IGF-I" mRNAs. Slot blot analysis of the RS-PCR products with internal oligonucleotide probes that specifically recognize IGF-I' or IGF-I" sequences revealed that only IGF-I' mRNA was present in follicles surrounding mature (stage VI) oocytes; neither IGF-I mRNA was present in follicles surrounding less mature oocytes (stages I and IV) or within oocytes or unfertilized eggs. After fertilization, IGF-I' mRNA was first detected during early organogenesis (stages 21-23), and increased during subsequent stages of development. To localize early IGF-I' expression, a stage 27 embryo was sliced into 24-microns cross-sections; RS-PCR and slot blot analysis were performed on RNA extracts from consecutive sections. IGF-I' mRNA was expressed in all sections, but was most abundant in the body region from which the visceral organs were developing. In contrast, to the early expression of IGF-I', IGF-I" mRNA was not detected until stage 41, a period corresponding to premetamorphic growth. Reverse PCR for Xenopus GH mRNA demonstrated that the onset of GH gene expression was coincident with the onset of IGF-I" gene expression (stage 41). These data suggest that the early expression of IGF-I' may be GH independent, whereas later expression of IGF-I" is GH dependent. We conclude that the two nonallelic IGF-I genes are expressed differentially in a stage-specific manner and suggest that IGF-I' may play an important role during early organogenesis, whereas IGF-I" may be important for premetamorphic growth.
为了研究胰岛素样生长因子-I(IGF-I)在早期胚胎发生过程中的潜在作用,我们使用了非洲爪蟾(Xenopus laevis),这是一种用于脊椎动物发育研究的通用模型。利用基于聚合酶链反应(PCR)的克隆策略,我们先前已鉴定出两种不同的非等位非洲爪蟾IGF-I基因(IGF-I'和IGF-I")。二者在成年肝脏中的表达量相似。我们现在报告使用一种改进的逆转录PCR方法,即RNA模板特异性PCR(RS-PCR),来检测单个卵母细胞和胚胎中的IGF-I信使核糖核酸(mRNA)。使用相同的引物对来扩增IGF-I'和IGF-I"的mRNA。用特异性识别IGF-I'或IGF-I"序列的内部寡核苷酸探针对RS-PCR产物进行狭缝印迹分析,结果显示,仅在成熟(VI期)卵母细胞周围的卵泡中存在IGF-I' mRNA;在较不成熟卵母细胞(I期和IV期)周围的卵泡中、卵母细胞内或未受精卵中均未检测到IGF-I mRNA。受精后,IGF-I' mRNA最早在早期器官发生阶段(21-23期)被检测到,并在随后的发育阶段增加。为了定位IGF-I'的早期表达,将一个27期胚胎切成24微米厚的横截面;对连续切片的RNA提取物进行RS-PCR和狭缝印迹分析。IGF-I' mRNA在所有切片中均有表达,但在内脏器官正在发育的身体区域中最为丰富。相比之下,与IGF-I'的早期表达不同,直到41期才检测到IGF-I" mRNA,这一时期对应于变态前生长阶段。非洲爪蟾生长激素(GH)mRNA的逆转录PCR显示,GH基因表达的起始与IGF-I"基因表达的起始(41期)一致。这些数据表明,IGF-I'的早期表达可能不依赖于GH,而IGF-I"的后期表达则依赖于GH。我们得出结论,这两个非等位IGF-I基因以阶段特异性方式差异表达,并表明IGF-I'可能在早期器官发生过程中发挥重要作用,而IGF-I"可能对变态前生长很重要。