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番茄多子叶基因座的遗传特征分析

Genetic characterization of the polycotyledon locus in tomato.

作者信息

Madishetty Kavitha, Bauer P, Sharada M S, Al-Hammadi A S A, Sharma R

机构信息

School of Life Sciences, University of Hyderabad, Hyderabad 500046, India.

出版信息

Theor Appl Genet. 2006 Aug;113(4):673-83. doi: 10.1007/s00122-006-0332-0. Epub 2006 Jun 29.

Abstract

Developmental mutants serve as a useful material to unravel the mechanisms necessary for organ development. The polycotyledon (poc) mutant of tomato, with multiple cotyledons in the seedling and varied phenotypic effects in the adult plant is one such mutant. Studies using physiological and anatomical methods in our lab suggest that POC is involved in the negative regulation of polar auxin transport, which is likely the reason for the pleiotropic phenotype in the mutant. Because of the physiological significance of the polycotyledon mutant described in this paper and also being first of its kind in tomato and also other plant species, we are using a map-based cloning approach to map the polycotyledon gene. Molecular mapping of this locus using segregating interspecific F2 mapping population localized polycotyledon gene close to TG424 marker on the long arm of chromosome 9. The closest marker mapped was a PCR marker identified in this study, E8A2 at a distance of 7.4 cM from the poc locus. The absence of tightly linked RAPD markers and the non-availability of more mapped markers in this region led us to initiate chromosome walk to polycotyledon gene. Both the flanking markers TG248 and E8A2 were used to screen the BAC library and a contig was developed for TG248 marker. The BAC-end sequences were analyzed for their use as RFLP markers to enrich this region for markers. Analysis of the BAC-end sequences revealed that poc is localized in the region surrounded by copia-like retrotransposon elements explaining the absence of markers in the euchromatin region on long arm of chromosome 9. Further studies identified two BAC-end sequences which mapped around the poc locus and also indicated very low physical versus genetic distance ratio in this region. The double mutant analyses of poc with the other two known polycotyledon mutants of tomato, pct and dem revealed allelism with pct; therefore, the poc mutant was named as pct1-2, and also the original pct mutant was renamed as pct1-1.

摘要

发育突变体是揭示器官发育所需机制的有用材料。番茄的多子叶(poc)突变体,幼苗中有多个子叶,成年植株有不同的表型效应,就是这样一种突变体。我们实验室使用生理和解剖学方法进行的研究表明,POC参与生长素极性运输的负调控,这可能是该突变体多效表型的原因。鉴于本文所述多子叶突变体的生理意义,且它在番茄及其他植物物种中尚属首例,我们正采用基于图谱的克隆方法来定位多子叶基因。利用分离的种间F2作图群体对该位点进行分子作图,将多子叶基因定位在9号染色体长臂上靠近TG424标记的位置。定位到的最紧密标记是本研究中鉴定的一个PCR标记E8A2,距离poc位点7.4厘摩。该区域缺乏紧密连锁的RAPD标记且可用的定位标记较少,这促使我们启动向多子叶基因的染色体步移。侧翼标记TG248和E8A2都用于筛选BAC文库,并为TG248标记构建了重叠群。分析BAC末端序列,以确定其作为RFLP标记的用途,从而在该区域富集标记。对BAC末端序列的分析表明,poc位于类copia逆转座子元件包围的区域,这解释了9号染色体长臂常染色质区域缺乏标记的原因。进一步研究鉴定出两个位于poc位点周围的BAC末端序列,还表明该区域物理距离与遗传距离的比率非常低。poc与番茄另外两个已知的多子叶突变体pct和dem的双突变分析表明,它与pct等位;因此,poc突变体被命名为pct1 - 2,原来的pct突变体则被重新命名为pct1 - 1。

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