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The alpha-tubulin gene family expressed during cell differentiation in Naegleria gruberi

机译:Naegleria gruberi细胞分化过程中表达的α-微管蛋白基因家族

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摘要

Genes that direct the programmed synthesis of flagellar alpha-tubulin during the differentiation of Naegleria gruberi from amebae to flagellates have been cloned, and found to be novel with respect to gene organization, sequence, and conservation. The flagellar alpha- tubulin gene family is represented in the genome by about eight homologous DNA segments that are exceptionally similar and yet are neither identical nor arrayed in a short tandem repeat. The coding regions of three of these genes have been sequenced, two from cDNA clones and one from an intronless genomic gene. These three genes encode an identical alpha-tubulin that is conserved relative to the alpha-tubulins of other organisms except at the carboxyl terminus, where the protein is elongated by two residues and ends in a terminal glutamine instead of the canonical tyrosine. In spite of the protein conservation, the Naegleria DNA sequence has diverged markedly from the alpha-tubulin genes of other organisms, a counterexample to the idea that tubulin genes are conserved. alpha-Tubulin mRNA homologous to this gene family has not been detected in amebae. This mRNA increases markedly in abundance during the first hour of differentiation, and then decreases even more rapidly with a half-life of approximately 8 min. The abundance of physical alpha-tubulin mRNA rises and subsequently falls in parallel with the abundance of translatable flagellar tubulin mRNA and with the in vivo rate of flagellar tubulin synthesis, which indicates that flagellar tubulin synthesis is directly regulated by the relative rates of transcription and mRNA degradation.
机译:已经克隆了指导将内生小球藻从变形虫变成鞭毛的过程中鞭毛α-微管蛋白的程序化合成的基因,并且发现在基因组织,序列和保守性方面是新颖的。鞭毛α-微管蛋白基因家族在基因组中由大约八个同源DNA片段表示,这些片段极为相似,但既不相同也不以短串联重复序列排列。这些基因中的三个的编码区已被测序,两个来自cDNA克隆,一个来自无内含子基因组基因。这三个基因编码的相同的α-微管蛋白相对于其他生物体的α-微管蛋白而言是保守的,除了在羧基末端,其中的蛋白质被两个残基延长,并在末端谷氨酰胺而不是典型的酪氨酸末端。尽管保留了蛋白质,但Naegleria DNA序列却与其他生物的α-微管蛋白基因明显不同,这是微管蛋白基因得以保守的想法的反例。尚未在amebae中检测到与该基因家族同源的α-TubulinmRNA。该mRNA在分化的第一小时内明显增加,然后以约8分钟的半衰期更快地下降。实际的α-微管蛋白mRNA的丰度升高,随后下降,与可翻译的鞭毛微管蛋白mRNA的丰度以及鞭毛微管蛋白合成的体内速率平行,这表明鞭毛微管蛋白的合成直接受转录和mRNA相对速率的调节。降解。

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