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番茄中同祖源的刺萼龙葵染色体的传递与重组

Transmission and recombination of homeologous Solanum sitiens chromosomes in tomato.

作者信息

Pertuzé Ricardo A, Ji Yuanfu, Chetelat Roger T

机构信息

C.M. Rick Tomato Genetics Resource Center, Department of Vegetable Crops, University of California, Davis, CA 95616, USA.

出版信息

Theor Appl Genet. 2003 Nov;107(8):1391-401. doi: 10.1007/s00122-003-1384-z. Epub 2003 Aug 16.

Abstract

The goal of the present experiments was to transfer the chromosomes of Solanum sitiens (syn. Solanum rickii) into cultivated tomato ( Lycopersicon esculentum). By crossing an allotetraploid L. esculentum x Solanum sitiens hybrid to sesquidiploid L. esculentum x S. lycopersicoides, a trigenomic hybrid (2n+14=38) was obtained. Analysis of the latter by GISH (genomic in situ hybridization) indicated it contained a full set of 12 S. sitiens chromosomes, plus two extras from S. lycopersicoides. This and other complex hybrids were pollinated with Lycopersicon pennellii-derived bridging lines to overcome unilateral incompatibility. A total of 40 progeny were recovered by embryo rescue, including diploids and aneuploids (up to 2n+8). In order to determine the origin of chromosomes and the location of introgressed segments, progeny were genotyped with RFLP markers. S. sitiens-specific markers on all chromosomes, except 6 and 11, were detected in the progeny. Several S. sitiens chromosomes were transmitted intact, either through chromosome addition (i.e., trisomics) or substitution (i.e., disomics). Recombination between S. sitiens and L. esculentum was detected on most chromosomes, in both diploid and aneuploid progeny. A monosomic alien addition line for S. sitiens chromosome 8 was identified, and the extra chromosome was stably transmitted to approximately 13% of the backcross progeny. This study demonstrates the feasibility of gene transfer from S. sitiens to L. esculentum through chromosome addition, substitution, and recombination in the progeny of complex aneuploid hybrids.

摘要

本实验的目的是将野生番茄(Solanum sitiens,同义名Solanum rickii)的染色体导入栽培番茄(Lycopersicon esculentum)。通过将异源四倍体番茄(L. esculentum)×野生番茄(S. sitiens)杂种与倍半二倍体番茄(L. esculentum)×多毛番茄(S. lycopersicoides)杂交,获得了一个三基因组杂种(2n + 14 = 38)。通过基因组原位杂交(GISH)对后者进行分析表明,它包含一套完整的12条野生番茄染色体,外加两条来自多毛番茄的额外染色体。用来自彭氏番茄(Lycopersicon pennellii)的桥梁品系对该杂种及其他复杂杂种进行授粉,以克服单向不亲和性。通过胚胎拯救共获得40个后代,包括二倍体和非整倍体(最多2n + 8)。为了确定染色体的来源和渐渗片段的位置,用限制性片段长度多态性(RFLP)标记对后代进行基因分型。在后代中检测到除6号和11号染色体外,所有染色体上的野生番茄特异性标记。几条野生番茄染色体通过染色体添加(即三体)或替换(即二体)完整地传递下去。在二倍体和非整倍体后代的大多数染色体上都检测到了野生番茄与栽培番茄之间的重组。鉴定出了一个野生番茄8号染色体的单体异附加系,这条额外的染色体稳定地传递给了大约13%的回交后代。本研究证明了通过复杂非整倍体杂种后代中的染色体添加、替换和重组,将野生番茄的基因转移到栽培番茄中的可行性。

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