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酵母中控制有丝分裂染色体传递的CHL基因的鉴定与遗传定位。

Identification and genetic mapping of CHL genes controlling mitotic chromosome transmission in yeast.

作者信息

Kouprina N, Tsouladze A, Koryabin M, Hieter P, Spencer F, Larionov V

机构信息

Institute of Cytology, Academy of Sciences of Russia, St Petersburg.

出版信息

Yeast. 1993 Jan;9(1):11-9. doi: 10.1002/yea.320090103.

Abstract

Eight independent chl (chromosome loss) mutants were isolated using yeast haploid strain disomic for chromosome III. In these mutants, chromosome III is lost during mitosis 50-fold more frequently than in the wild-type strains. chl mutants are also incapable of stable maintenance of circular and linear artificial chromosomes. Seven of the eight mutations are recessive, and one is semidominant. Complementation tests placed these mutants into six complementation groups (chl11 through chl16). Based on tetrad analysis, chl12, chl14 and chl15 correspond to mutations in single nuclear genes. Tetrad analysis of the other mutants was not possible due to poor spore viability. Complementation analysis was also carried out between collection of chl mutants and ctf mutants (chromosome transmission fidelity) (Spencer et al., 1990). The chl3, chl4, chl8, chl12 and chl15 mutants were unable to complement ctf3, ctf17, ctf12, ctf18 and ctf4, respectively. Three CHL genes were mapped by tetrad analysis. The CHL3 gene is placed on the right arm of chromosome XII, between the ILV5 (33.3 cM) and URA4 (21.8 cM) loci. The CHL10 gene is located on the left arm of chromosome VI, 12.5 cM from the centromere. The CHL15 gene is tightly linked to the KAR3 marker of the right arm of chromosome XVI (8.8 cM). The mapping data indicate that these three genes differ from other genes known to affect chromosome stability in mitosis. Therefore, the total number of the CHL genes identified (including those described by us earlier) is 13 (CHL1-CHL10, CHL12, CHL14 and CHL15).

摘要

利用酵母三号染色体双体单倍体菌株分离出8个独立的chl(染色体丢失)突变体。在这些突变体中,三号染色体在有丝分裂期间丢失的频率比野生型菌株高50倍。chl突变体也无法稳定维持环状和线性人工染色体。8个突变中有7个是隐性的,1个是半显性的。互补测验将这些突变体分为6个互补群(chl11至chl16)。基于四分体分析,chl12、chl14和chl15对应单核基因突变。由于孢子活力差,无法对其他突变体进行四分体分析。还对chl突变体集合与ctf突变体(染色体传递保真度)进行了互补分析(斯宾塞等人,1990年)。chl3、chl4、chl8、chl12和chl15突变体分别无法与ctf3、ctf17、ctf12、ctf18和ctf4互补。通过四分体分析定位了3个CHL基因。CHL3基因位于十二号染色体右臂,在ILV5(33.3 cM)和URA4(21.8 cM)位点之间。CHL10基因位于六号染色体左臂,距着丝粒12.5 cM。CHL15基因与十六号染色体右臂的KAR3标记紧密连锁(8.8 cM)。定位数据表明,这三个基因与已知影响有丝分裂中染色体稳定性的其他基因不同。因此,已鉴定的CHL基因总数(包括我们之前描述的那些)为13个(CHL1-CHL10、CHL12、CHL14和CHL15)。

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