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Expression and functional analysis of TaASY1 during meiosis of bread wheat (Triticum aestivum)

机译:TaASY1在面包小麦减数分裂过程中的表达及功能分析

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Background Pairing and synapsis of homologous chromosomes is required for normal chromosome segregation and the exchange of genetic material via recombination during meiosis. Synapsis is complete at pachytene following the formation of a tri-partite proteinaceous structure known as the synaptonemal complex (SC). In yeast, HOP1 is essential for formation of the SC, and localises along chromosome axes during prophase I. Homologues in Arabidopsis (AtASY1), Brassica (BoASY1) and rice (OsPAIR2) have been isolated through analysis of mutants that display decreased fertility due to severely reduced synapsis of homologous chromosomes. Analysis of these genes has indicated that they play a similar role to HOP1 in pairing and formation of the SC through localisation to axial/lateral elements of the SC. Results The full length wheat cDNA and genomic clone, TaASY1, has been isolated, sequenced and characterised. TaASY1 is located on chromosome Group 5 and the open reading frame displays significant nucleotide sequence identity to OsPAIR2 (84%) and AtASY1 (63%). Transcript and protein analysis showed that expression is largely restricted to meiotic tissue, with elevated levels during the stages of prophase I when pairing and synapsis of homologous chromosomes occur. Immunolocalisation using transmission electron microscopy showed TaASY1 interacts with chromatin that is associated with both axial elements before SC formation as well as lateral elements of formed SCs. Conclusion TaASY1 is a homologue of ScHOP1, AtASY1 and OsPAIR2 and is the first gene to be isolated from bread wheat that is involved in pairing and synapsis of homologous chromosomes.
机译:背景正常染色体的分离和减数分裂过程中通过重组进行遗传物质交换需要同源染色体的配对和突触。在被称为突触复合物(SC)的三部分蛋白质结构形成之后,在粗线中突触完成。在酵母中,HOP1是形成SC所必需的,并且在前期I期间沿着染色体轴定位。通过分析显示由于生育力降低而导致的生育力降低的拟南芥(AtASY1),芸苔属植物(BoASY1)和水稻(OsPAIR2)的同源物严重减少了同源染色体的突触。对这些基因的分析表明,它们通过定位于SC的轴向/侧向元件,在SC的配对和形成中与HOP1发挥相似的作用。结果已分离,测序和鉴定了全长小麦cDNA和基因组克隆TaASY1。 TaASY1位于第5组染色体上,开放阅读框显示与OsPAIR2(84%)和AtASY1(63%)显着的核苷酸序列同一性。转录本和蛋白质分析表明,表达主要限于减数分裂组织,在同源染色体的配对和突触发生的前期I阶段水平升高。使用透射电子显微镜的免疫定位显示TaASY1与染色质相互作用,染色质与SC形成之前的轴向元素以及形成的SC的横向元素都相关。结论TaASY1是ScHOP1,AtASY1和OsPAIR2的同源物,是从面包小麦中分离到的第一个与同源染色体配对和突触有关的基因。

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