Breckler J, Au K, Cheng J, Hasson T, Burnside B
Department of Biology, San Francisco State University, San Francisco, CA, USA.
Exp Eye Res. 2000 Jan;70(1):121-34. doi: 10.1006/exer.1999.0758.
Several forms of sensory deficit have been associated with unconventional myosin defects in humans and other animals. Normal hearing in mammals has been shown to require functional myosin VI (Avraham et al., 1995) and myosin VIIA (Gibson et al., 1995; Liu et al., 1997), and the combined blindness and deafness of Usher syndrome type IB has been shown to be produced by specific defects in myosin VIIA (Weil et al., 1997). Here we report the cloning and characterization of two distinct myosin VI isoforms (FMVIA and FMVIB) initially identified in a degenerate PCR screen of retinal cDNA from the striped bass, Morone saxatilis. Open reading frames for FMVIA and FMVIB encode predicted proteins of 1304 and 1270 amino acids respectively, which are 83% identical at the amino acid level. Both fish isoforms are likewise approximately 83-86% identical to mammalian class VI myosins (Hasson and Mooseker, 1994). Northern blot analysis revealed that FMVIA mRNA is broadly expressed and most abundant in kidney, a pattern similar to that previously reported for mammalian myosin VI. FMVIB expression is dramatically more abundant in retina than in any other tissue examined. Antibodies directed against pig myosin VI (Hasson and Mooseker, 1994) detect a doublet at approximately 150 kDa in bass retina and RPE. Since both fish VIA and VIB isoforms share high sequence identity with pig myosin VI within the domain used for antibody production, it seems likely that this antibody crossreacts with both FMVIA and FMVIB. Immunocytochemistry with this same affinity-purified rabbit anti-myosin VI antibody shows that myosin VI isoforms are primarily localized in photoreceptors, horizontal cells and Müller cells in both fish and primate retinas. This report is the first demonstration that two myosin VI genes are expressed in the same organism and the same cell type (RPE). The relatively high abundance of FMVIB expression in retina suggests that it may play an important role in retinal motility events.
在人类和其他动物中,几种形式的感觉缺陷与非常规肌球蛋白缺陷有关。哺乳动物的正常听力已被证明需要功能性肌球蛋白VI(阿夫拉罕等人,1995年)和肌球蛋白VIIA(吉布森等人,1995年;刘等人,1997年),而1B型Usher综合征的失明和失聪合并症已被证明是由肌球蛋白VIIA的特定缺陷引起的(韦尔等人,1997年)。在这里,我们报告了两种不同的肌球蛋白VI同工型(FMVIA和FMVIB)的克隆和特性,它们最初是在条纹鲈(Morone saxatilis)视网膜cDNA的简并PCR筛选中鉴定出来的。FMVIA和FMVIB的开放阅读框分别编码预测的1304和1270个氨基酸的蛋白质,它们在氨基酸水平上有83%的同一性。这两种鱼类同工型与哺乳动物VI类肌球蛋白同样也有大约83%-86%的同一性(哈森和穆斯克,1994年)。Northern印迹分析显示,FMVIA mRNA广泛表达,在肾脏中最为丰富,这种模式与先前报道的哺乳动物肌球蛋白VI相似。FMVIB在视网膜中的表达明显比在任何其他检测的组织中丰富得多。针对猪肌球蛋白VI的抗体(哈森和穆斯克,1994年)在鲈鱼视网膜和视网膜色素上皮中检测到一条约150 kDa的双峰。由于两种鱼类VIA和VIB同工型在用于产生抗体的结构域内与猪肌球蛋白VI具有高度的序列同一性,因此这种抗体似乎可能与FMVIA和FMVIB都发生交叉反应。用这种相同的亲和纯化兔抗肌球蛋白VI抗体进行免疫细胞化学分析表明,肌球蛋白VI同工型主要定位于鱼类和灵长类动物视网膜的光感受器、水平细胞和米勒细胞中。本报告首次证明了两个肌球蛋白VI基因在同一生物体和同一细胞类型(视网膜色素上皮)中表达。FMVIB在视网膜中相对较高的表达丰度表明它可能在视网膜运动事件中起重要作用。