Smas C M, Green D, Sul H S
Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts 02115.
Biochemistry. 1994 Aug 9;33(31):9257-65. doi: 10.1021/bi00197a029.
Preadipocyte factor 1 (pref-1), a member of the EGF-like protein family, is a transmembrane protein with six tandem EGF-like repeats in the putative extracellular domain. Expression of pref-1 is abolished during the in vitro differentiation of 3T3-L1 preadipocytes to adipocytes, and constitutive expression of pref-1 in preadipocytes inhibits their differentiation [Smas, C.M., & Sul, H.S. (1993) Cell 73, 725-734]. In the present studies, we have isolated and characterized genomic clones for pref-1 and have identified multiple pref-1 transcripts generated by alternate splicing. The pref-1 gene consists of five exons and four introns spanning approximately 7.3 kb. By primer extension analysis, the transcription start site was determined to be 169 bp upstream from the translation initiation codon. We have identified functional promoter sequences by transient transfection using a 2.1 kb fragment of the pref-1 5' flanking region linked to a luciferase gene; the pref-1-luciferase fusion gene construct gave 20-fold higher promoter activity as compared to the promoterless vector. Analysis of exon-intron junctions reveals that unlike the majority of the mammalian EGF-like genes, EGF-like repeats of pref-1 are not encoded by discrete exons. Through RT-PCR and the isolation and analysis of multiple pref-1 cDNA clones, we have identified, in addition to full-length pref-1, five alternately spliced forms with various in-frame deletions of all or a part of the sixth EGF-like repeat, juxta-membrane, and predicted transmembrane domains.(ABSTRACT TRUNCATED AT 250 WORDS)
前脂肪细胞因子1(Pref-1)是表皮生长因子(EGF)样蛋白家族的成员,是一种跨膜蛋白,在假定的细胞外结构域中有六个串联的EGF样重复序列。在3T3-L1前脂肪细胞体外分化为脂肪细胞的过程中,Pref-1的表达被消除,并且前脂肪细胞中Pref-1的组成型表达会抑制其分化[Smas, C.M., & Sul, H.S. (1993) Cell 73, 725 - 734]。在本研究中,我们分离并鉴定了Pref-1的基因组克隆,并确定了由可变剪接产生的多种Pref-1转录本。Pref-1基因由五个外显子和四个内含子组成,跨度约为7.3 kb。通过引物延伸分析,确定转录起始位点位于翻译起始密码子上游169 bp处。我们通过使用与荧光素酶基因相连的Pref-1 5'侧翼区域的2.1 kb片段进行瞬时转染,确定了功能性启动子序列;与无启动子载体相比,Pref-1-荧光素酶融合基因构建体的启动子活性高20倍。外显子-内含子连接分析表明,与大多数哺乳动物EGF样基因不同,Pref-1的EGF样重复序列不是由离散的外显子编码的。通过逆转录聚合酶链反应(RT-PCR)以及多个Pref-1 cDNA克隆的分离和分析,我们除了鉴定出全长Pref-1外,还发现了五种可变剪接形式,这些形式在第六个EGF样重复序列、近膜区和预测的跨膜结构域的全部或部分存在各种框内缺失。(摘要截短于250字)