Brannan C I, Dees E C, Ingram R S, Tilghman S M
Howard Hughes Medical Institute, Princeton University New Jersey 08544.
Mol Cell Biol. 1990 Jan;10(1):28-36. doi: 10.1128/mcb.10.1.28-36.1990.
The mouse H19 gene was identified as an abundant hepatic fetal-specific mRNA under the transcriptional control of a trans-acting locus termed raf. The protein this gene encoded was not apparent from an analysis of its nucleotide sequence, since the mRNA contained multiple translation termination signals in all three reading frames. As a means of assessing which of the 35 small open reading frames might be important to the function of the gene, the human H19 gene was cloned and sequenced. Comparison of the two homologs revealed no conserved open reading frame. Cellular fractionation showed that H19 RNA is cytoplasmic but not associated with the translational machinery. Instead, it is located in a particle with a sedimentation coefficient of approximately 28S. Despite the fact that it is transcribed by RNA polymerase II and is spliced and polyadenylated, we suggest that the H19 RNA is not a classical mRNA. Instead, the product of this unusual gene may be an RNA molecule.
小鼠H19基因被鉴定为一种丰富的肝脏胎儿特异性mRNA,受一个称为raf的反式作用位点的转录控制。从该基因的核苷酸序列分析中未发现其编码的蛋白质,因为该mRNA在所有三个阅读框中都包含多个翻译终止信号。作为评估35个小开放阅读框中哪一个可能对该基因功能重要的一种方法,对人类H19基因进行了克隆和测序。两种同源物的比较未发现保守的开放阅读框。细胞分级分离显示H19 RNA位于细胞质中,但与翻译机制无关。相反,它存在于沉降系数约为28S的颗粒中。尽管它由RNA聚合酶II转录、剪接和聚腺苷酸化,但我们认为H19 RNA不是经典的mRNA。相反,这个不寻常基因的产物可能是一种RNA分子。