Murray M T, White K, Munro H N
Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge 02139.
Proc Natl Acad Sci U S A. 1987 Nov;84(21):7438-42. doi: 10.1073/pnas.84.21.7438.
Ferritin stores iron within a protein shell consisting of 24 subunits of two types, heavy (H) and light (L). According to Southern blotting, the rat genome contains four copies homologous to the H-subunit cDNA (H cDNA). To determine whether only one of these is expressed, H cDNAs isolated from rat liver and heart mRNAs were compared and found to share identical nucleotide sequences. Next, genomic clones for three of the four rat H-subunit loci were isolated. Two were classical processed pseudogenes, whereas the third contained an expressed gene. RNase intron mapping of this expressed gene generated the same exon protection pattern when total RNA from rat liver or heart was used, indicating that this gene accounts for most or all of the H-subunit mRNAs (H mRNAs) in these tissues. Comparison of the expressed rat H-subunit gene (H gene) structure with published sequences for other species displays considerable conservation. The coding sequence of the rat H gene predicts 95% similarity to the human amino acid sequence, thus being more highly conserved than the L-subunit sequence of these species. Near the cap region of the 5' untranslated region, the rat H mRNA displays a 28-nucleotide sequence that is almost totally conserved in the corresponding region of the human, bullfrog, and chicken H mRNA and is also faithfully represented in the rat and human L-subunit mRNAs (L mRNAs), thus making this sequence a prime candidate for involvement in the known translational regulation of both subunits by iron. In the 5' flanking region, partially conserved sequences common to H gene and L-subunit gene (L gene) of the rat may be involved in transcriptional regulation by iron, whereas those conserved only in the H gene of man and the rat imply that other factors may independently control H-subunit regulation.
铁蛋白将铁储存在一个由重链(H)和轻链(L)两种类型的24个亚基组成的蛋白质外壳内。根据Southern印迹法,大鼠基因组包含四个与H亚基cDNA(H cDNA)同源的拷贝。为了确定这些拷贝中是否只有一个表达,对从大鼠肝脏和心脏mRNA中分离的H cDNA进行了比较,发现它们具有相同的核苷酸序列。接下来,分离了四个大鼠H亚基基因座中的三个的基因组克隆。其中两个是典型的加工假基因,而第三个包含一个表达基因。当使用来自大鼠肝脏或心脏的总RNA时,该表达基因的核糖核酸酶内含子图谱产生了相同的外显子保护模式,表明该基因占这些组织中大多数或所有H亚基mRNA(H mRNA)。将表达的大鼠H亚基基因(H基因)结构与其他物种的已发表序列进行比较,显示出相当程度的保守性。大鼠H基因的编码序列预测与人氨基酸序列的相似性为95%,因此比这些物种的L亚基序列保守性更高。在5'非翻译区的帽区附近,大鼠H mRNA显示出一个28个核苷酸的序列,该序列在人、牛蛙和鸡的H mRNA的相应区域几乎完全保守,并且在大鼠和人的L亚基mRNA(L mRNA)中也忠实地呈现,因此使该序列成为参与已知的铁对两个亚基翻译调控的主要候选序列。在5'侧翼区,大鼠H基因和L亚基基因(L基因)共有的部分保守序列可能参与铁的转录调控,而仅在人和大鼠的H基因中保守的序列意味着其他因素可能独立控制H亚基的调控。