Li X, Wistow G J, Piatigorsky J
Section on Molecular Genetics, National Eye Institute, National Institutes of Health, Bethesda, MD 20892.
Biochim Biophys Acta. 1995 Mar 14;1261(1):25-34. doi: 10.1016/0167-4781(94)00211-k.
delta-Crystallin is the major component of the lenses of most birds and reptiles. In the chicken there are two closely linked, tandemly oriented genes. Almost all of the delta-crystallin of the embryonic chicken lens is produced by the 5' delta 1 gene. This high lens activity has been attributed to an enhancer in intron 3. The 3' delta 2 gene encodes the enzyme argininosuccinate lyase (ASL) which is expressed at a low level in the chicken lens. Both chicken delta-crystallin genes are also expressed slightly in heart and brain, with ASL/delta 2 predominating over delta 1. In the duck (Anas platyrhynchos), ASL/delta 2-crystallin serves as both enzyme and crystallin, resulting in very high levels of ASL activity in the lens. Here we show by genomic cloning that the ASL/delta- crystallin locus is highly conserved between duck and chicken, with the two duck delta-crystallin genes closely linked in tandem. The 4.6 kbp intergenic spacer in the duck locus is 79% identical to the 4 kbp chicken spacer, except for the existence of a 615 bp CR1 element, highly reiterated in the duck genome, 1.8 kbp upstream of the duck ASL/delta 2 gene. The CR1 sequence is a truncated LINE element containing the 3' half of an open reading frame for a retroviral pol-like reverse transcriptase. Sequence analysis revealed (i) that intron 3 of the duck ASL/delta 2 gene is very similar (80%) to intron 3 of the chicken delta 1 and ASL/delta 2 genes, especially in the region of the chicken delta 1 enhancer core (93% identical) and (ii) that the 3' boundary of exon 2 of the duck ASL/delta 2 gene has undergone a recent splice-site slippage event, resulting in a two amino acid insertion in the encoded polypeptide. Finally, reverse transcription/polymerase chain reaction experiments established that both delta-crystallin genes are equally expressed to a high level in the embryonic duck lens; by contrast, both delta-crystallin genes produce a low amount of mRNA in the heart and brain of the embryonic duck, with the enzymatically active ASL/delta 2 being preferentially expressed.
δ-晶体蛋白是大多数鸟类和爬行动物晶状体的主要成分。在鸡中,有两个紧密连锁、串联排列的基因。胚胎期鸡晶状体中几乎所有的δ-晶体蛋白都是由5'δ1基因产生的。这种高晶状体活性归因于内含子3中的一个增强子。3'δ2基因编码精氨琥珀酸裂解酶(ASL),该酶在鸡晶状体中低水平表达。鸡的两个δ-晶体蛋白基因在心脏和大脑中也有轻微表达,其中ASL/δ2的表达量高于δ1。在鸭(绿头鸭)中,ASL/δ2-晶体蛋白兼具酶和晶体蛋白的功能,导致晶状体中ASL活性水平非常高。在这里,我们通过基因组克隆表明,鸭和鸡的ASL/δ-晶体蛋白基因座高度保守,鸭的两个δ-晶体蛋白基因紧密串联。鸭基因座中的4.6kbp基因间隔区与鸡的4kbp间隔区有79%的同一性,除了在鸭ASL/δ2基因上游1.8kbp处存在一个在鸭基因组中高度重复的615bp CR1元件。CR1序列是一个截短的长散在核元件,包含逆转录病毒pol样逆转录酶开放阅读框的3'半部分。序列分析显示:(i)鸭ASL/δ2基因的内含子3与鸡δ1和ASL/δ2基因的内含子3非常相似(80%),特别是在鸡δ1增强子核心区域(93%相同);(ii)鸭ASL/δ2基因外显子2的3'边界最近发生了剪接位点滑动事件,导致编码多肽中插入了两个氨基酸。最后,逆转录/聚合酶链反应实验证实,两个δ-晶体蛋白基因在胚胎期鸭晶状体中均高水平且等量表达;相比之下,两个δ-晶体蛋白基因在胚胎期鸭的心脏和大脑中产生的mRNA量较低,其中具有酶活性的ASL/δ2优先表达。