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酿酒酵母十二号染色体上rDNA簇区域的克隆大小变异

Clonal size-variation of rDNA cluster region on chromosome XII of Saccharomyces cerevisiae.

作者信息

Chindamporn A, Iwaguchi S, Nakagawa Y, Homma M, Tanaka K

机构信息

Laboratory of Medical Mycology, Nagoya University School of Medicine, Japan.

出版信息

J Gen Microbiol. 1993 Jul;139(7):1409-15. doi: 10.1099/00221287-139-7-1409.

Abstract

Using pulsed-field gel electrophoresis (PFGE), we have demonstrated clonal variation in the size of chromosome XII in a diploid strain of Saccharomyces cerevisiae X2180-2D. The sizes of the two chromosome XII homologues were very different: 2600 (L-type) and 1450 kb (S-type). The frequency with which we detected clonal size variation in the diploid, compared to that of the parental clones, was about 15-50% of the progeny clones and the range of the size variation of the homologues was 2580-2680 kb (L-type) and 1340-1500 kb (S-type), respectively. The homologue of the L-type appeared to be more frequently variable than that of the S-type. The size variation was shown to be derived from size changes in the rDNA cluster region, which is present in chromosome XII, by digesting the chromosome with XhoI, whose cutting site is not present in a rDNA repeat unit, and hybridizing to rDNA probes. The clonal size variation was also investigated in haploids from spores after meiosis. The L-type and S-type chromosomes segregated 2:2 in an ascus and the sizes of all the S-type chromosomes were shifted up, compared to the original diploid, though the L-type ones were stable. The S-type sizes of 1340, 1450 and 1780 kb in the original diploids changed into the ranges of 1475-1610 kb, 1520-1680 kb and 1820-2010 kb, respectively, in the segregants. Furthermore, we observed that the size of S-type chromosomes in haploid cells was gradually increasing in mitosis during successive subcultures.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用脉冲场凝胶电泳(PFGE),我们在酿酒酵母X2180 - 2D的二倍体菌株中证实了第十二号染色体大小的克隆变异。两条第十二号染色体同源物的大小差异很大:2600 kb(L型)和1450 kb(S型)。与亲代克隆相比,我们在二倍体中检测到克隆大小变异的频率约为子代克隆的15% - 50%,同源物大小变异范围分别为2580 - 2680 kb(L型)和1340 - 1500 kb(S型)。L型同源物似乎比S型更频繁地发生变异。通过用XhoI消化染色体(其切割位点不在rDNA重复单元中)并与rDNA探针杂交,表明大小变异源自第十二号染色体上rDNA簇区域的大小变化。还对减数分裂后孢子形成的单倍体中的克隆大小变异进行了研究。L型和S型染色体在一个子囊中以2:2分离,与原始二倍体相比,所有S型染色体的大小都上移了,尽管L型染色体是稳定的。原始二倍体中1340、1450和1780 kb的S型大小在分离后代中分别变为1475 - 1610 kb、1520 - 1680 kb和1820 - 2010 kb的范围。此外,我们观察到在连续传代培养的有丝分裂过程中,单倍体细胞中S型染色体的大小逐渐增加。(摘要截断于250字)

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