Genes in the germline (micronuclear) genome of hypotrichous ciliates are interrupted by multiple, short, non-coding, AT-rich sequences called internal eliminated segments, or IESs. During conversion of a micronucleus to a somatic nucleus (macronucleus) after cell mating, all IESs are excised from the germline genes and the gene segments, called macronuclear-destined segments, or MDSs, are spliced. Excision of the approximately 150 000 IESs from a haploid germline genome in Oxytricha nova requires approximately 150 000 recombinant events. In three of 10 genes the MDSs are scrambled. During macronuclear development the MDSs are unscrambled, possibly by folding of the DNA to allow MDSs to ligate in the correct order. The nine MDSs in the actin I gene of O.nova are scrambled in the random order, 3-4-6-5-7-9-2-1-8, and MDS 2 is inverted. The 14 MDSs in the alphaTP gene of O.nova and Stylonychia mytilus are scrambled in the non-random order, 1-3-5-7-9-11-2-4-6-8-10-12-13-14. The 45 MDSs in the DNA pol alpha gene are non-randomly scrambled into an odd/even series, with an inversion of one-third of the gene. Additional IESs have been inserted into these three genes during evolution of Oxytricha trifallax, slightly modifying scrambling patterns. The non-random scrambled patterns in the alphaTP and DNA pol alpha genes are explained by multiple, simultaneous IES insertions. The randomly scrambled pattern in the actin I gene may arise from an initially non-randomly scrambled pattern by recombination among multiple IESs. Alternatively, IESs inserted sporadically (individually) in a non-scrambled configuration might subsequently recombine, converting a non-scrambled gene into a randomly scrambled one. IESs shift along a DNA molecule, most likely as a result of mutations at MDS/IES junctions. Shifting of IESs has the effect of 'transferring' nucleotides from one MDS to another, but does not change the overall sequence of nucleotides in the combined MDSs. In addition to shifting in position, IESs accumulate mutations at a high rate and increase and decrease in length within a species and during speciation. The phenomena of IESs and of MDS scrambling represent remarkable flexibility of the hypotrich genome, possibly reflecting a process of MDS shuffling that facilitates the evolution of genes.
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机译:纤毛虫纤毛(微核)基因组中的基因被称为内部消除区段或IES的多个短的,非编码的,富含AT的序列打断。细胞交配后,在将微核转化为体核(巨核)的过程中,从种系基因中切除了所有IES,并剪接了称为大核定点的片段或MDS的基因片段。从Oxytricha nova的单倍体种系基因组中切除大约15万个IES需要大约15万个重组事件。在10个基因中的3个中,MDS被打乱。在大核发育过程中,MDS可能不加扰,可能是通过折叠DNA使MDS以正确的顺序结扎。 O.nova的肌动蛋白I基因中的9个MDS以3-4-6-5-7-9-2-1-8的随机顺序被扰乱,并且MDS 2被倒置。 O.nova和Stylonychia mytilus的alphaTP基因中的14个MDS按非随机顺序扰乱1-3-5-7-9-11-2-4-6-8-10-12-13-14 。 DNA pol alpha基因中的45个MDS被非随机地扰乱成奇/偶数序列,而该基因的三分之一被倒置。在Oxytricha trifallax的进化过程中,其他IES被插入到这三个基因中,从而稍微改变了加扰模式。 alphaTP和DNA pol alpha基因中的非随机加扰模式是通过同时插入多个IES来解释的。肌动蛋白I基因中的随机加扰模式可以通过多个IES之间的重组源自最初的非随机加扰模式。或者,以非加扰的结构偶发地(个别地)插入的IES可能随后重组,将一个非加扰的基因转化为一个随机加扰的基因。 IES沿着DNA分子移动,这很可能是MDS / IES连接处突变的结果。 IES的移位具有将核苷酸从一个MDS“转移”到另一个MDS的作用,但不会改变组合MDS中核苷酸的整体序列。除了位置的改变外,IES还以高速率积累突变,并在物种内和物种形成过程中增加和减少长度。 IESs和MDS加扰现象代表了hypotrich基因组的显着灵活性,这可能反映了MDS改组过程促进了基因的进化。
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