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Erythroid anion transporter assembly is mediated by a developmentally regulated recruitment onto a preassembled membrane cytoskeleton

机译:红血球阴离子转运蛋白的组装是由发育调控的募集介导到预组装的膜细胞骨架上的

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摘要

Analysis of the expression and assembly of the anion transporter by metabolic pulse-chase and steady-state protein and RNA measurements reveals that the extent of association of band 3 with the membrane cytoskeleton varies during chicken embryonic development. Pulse-chase studies have indicated that band 3 polypeptides do not associate with the membrane cytoskeleton until they have been transported to the plasma membrane. At this time, band 3 polypeptides are slowly recruited, over a period of hours, onto a preassembled membrane cytoskeletal network and the extent of this cytoskeletal assembly is developmentally regulated. Only 3% of the band 3 polypeptides are cytoskeletal-associated in 4-d erythroid cells vs. 93% in 10-d erythroid cells and 36% in 15-d erythroid cells. This observed variation appears to be regulated primarily at the level of recruitment onto the membrane cytoskeleton rather than by different transport kinetics to the membrane or differential turnover of the soluble and insoluble polypeptides and is not dependent upon the lineage or stage of differentiation of the erythroid cells. Steady-state protein and RNA analyses indicate that the low levels of cytoskeletal band 3 very early in development most likely result from limiting amounts of ankyrin and protein 4.1, the membrane cytoskeletal binding sites for band 3. As embryonic development proceeds, ankyrin and protein 4.1 levels increase with a concurrent rise in the level of cytoskeletal band 3 until, on day 10 of development, virtually all of the band 3 polypeptides are cytoskeletal bound. After day 10, the levels of total and cytoskeletal band 3 decline, whereas ankyrin and protein 4.1 continue to accumulate until day 18, indicating that the cytoskeletal association of band 3 is not regulated solely by the availability of membrane cytoskeletal binding sites at later stages of development. Thus, multiple mechanisms appear to regulate the recruitment of band 3 onto the erythroid membrane cytoskeleton during chicken embryonic development.
机译:通过代谢脉冲追踪,稳态蛋白质和RNA测量对阴离子转运蛋白的表达和组装进行分析,发现在鸡胚胎发育过程中,条带3与膜细胞骨架的结合程度有所不同。脉冲追踪研究表明,带3多肽直到被转运到质膜后才与膜细胞骨架结合。此时,在几个小时内,将带状3多肽缓慢募集到预先组装的膜细胞骨架网络上,并通过发育调节该细胞骨架组装的程度。带3的多肽中只有3%在4-d红细胞中与细胞骨架相关,而在10d红细胞中为93%,在15d红细胞中为36%。这种观察到的变异似乎主要在募集到膜细胞骨架上的水平上调节,而不是通过向膜的不同运输动力学或可溶性和不溶性多肽的不同转换来调节,并且不取决于红系细胞的谱系或分化阶段。稳态蛋白质和RNA分析表明,发育初期细胞骨架带3的低水平很可能是由于限制了锚蛋白和蛋白质4.1的含量,限制了乐队3的膜细胞骨架结合位点。随着胚胎发育的进行,锚蛋白和蛋白质4.1伴随着细胞骨架带3水平的升高,其水平增加,直到发展的第10天,实际上所有带3多肽都被细胞骨架结合。在第10天后,总带和细胞骨架3带的水平下降,而锚蛋白和蛋白4.1继续积累直至第18天,这表明,在带的后期,膜3的细胞骨架结合位点的可用性并不仅仅调节带3的细胞骨架结合。发展。因此,在鸡胚胎发育过程中,似乎有多种机制调节条带3在红系膜细胞骨架上的募集。

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