Centro de Biologia, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Theor Appl Genet. 1973 Jan;43(3-4):174-81. doi: 10.1007/BF00306568.
Measurements of distances between telocentric chromosomes, either homologous or representing the opposite arms of a metacentric chromosome (complementary telocentrics), were made at metaphase in root tip cells of common wheat carrying two homologous pairs of complementary telocentrics of chromosome 1 B or 6 B (double ditelosomic 1 B or 6 B). The aim was to elucidate the relative locations of the telocentric chromosomes within the cell. The data obtained strongly suggest that all four telocentrics of chromosome 1 B or 6 B are spacially and simultaneously co-associated. In plants carrying two complementary (6 B (S) and 6 B (L)) and a non-related (5 B (L)) telocentric, only the complementary chromosomes were found to be somatically associated. It is thought, therefore, that the somatic association of chromosomes may involve more than two chromosomes in the same association and, since complementary telocentrics are as much associated as homologous, that the homology between centromeres (probably the only homologous region that exists between complementary telocentrics) is a very important condition for somatic association of chromosomes. The spacial arrangement of chromosomes was studied at anaphase and prophase and the polar orientation of chromosomes at prophase was found to resemble anaphase orientation. This was taken as good evidence for the maintenance of the chromosome arrangement - the Rabl orientation - and of the peripheral location of the centromere and its association with the nuclear membrane. Within this general arrangement homologous telocentric chromosomes were frequently seen to have their centromeres associated or directed towards each other. The role of the centromere in somatic association as a spindle fibre attachment and chromosome binder is discussed. It is suggested that for non-homologous chromosomes to become associated in root tips, the only requirement needed should be the homology of centromeres such as exists between complementary telocentrics, or, as a possible alternative, common repeated sequences of DNA molecules around the centromere region.
测量着丝粒染色体之间的距离,无论是同源的还是代表着中着丝粒染色体的相反臂的(互补着丝粒),在携带一对同源的 1B 或 6B 染色体的互补着丝粒(双单价体 1B 或 6B)的小麦根尖细胞中期进行。目的是阐明细胞内着丝粒染色体的相对位置。所得数据强烈表明,1B 或 6B 的所有四个着丝粒染色体在空间上同时共同关联。在携带两个互补的(6B(S) 和 6B(L))和一个非相关的(5B(L))着丝粒的植物中,只有互补染色体被发现是体细胞相关的。因此,人们认为染色体的体细胞关联可能涉及同一关联中的两个以上染色体,并且由于互补着丝粒与同源染色体一样多相关,因此着丝粒之间的同源性(可能是互补着丝粒之间存在的唯一同源区域)是染色体体细胞关联的一个非常重要的条件。在后期和前期研究了染色体的空间排列,并且发现前期染色体的极向类似于后期取向。这被认为是维持染色体排列(Rabl 取向)和着丝粒的外周位置及其与核膜的关联的良好证据。在这个一般排列中,同源的着丝粒染色体经常被观察到它们的着丝粒相关或彼此指向。讨论了着丝粒在作为纺锤体纤维附着点和染色体结合物的体细胞关联中的作用。有人认为,为了使非同源染色体在根尖中相关联,唯一需要的条件应该是着丝粒的同源性,就像在互补着丝粒之间存在的那样,或者,作为一种可能的替代方案,在着丝粒区域周围存在共同的 DNA 分子重复序列。