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莱茵衣藻核基因组中的同源重组

Homologous recombination in the nuclear genome of Chlamydomonas reinhardtii.

作者信息

Sodeinde O A, Kindle K L

机构信息

Plant Science Center, Cornell University, Ithaca, NY 14853.

出版信息

Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):9199-203. doi: 10.1073/pnas.90.19.9199.

DOI:10.1073/pnas.90.19.9199
PMID:8415677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC47530/
Abstract

Nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii has thus far been characterized by integration of the introduced DNA into nonhomologous sites. In this study, the occurrence of homologous recombination events during transformation was investigated with the intent of developing strategies for gene targeting and gene disruption. Homologous recombination was monitored by using nonfunctional 5' and 3' deletion derivatives of the wild-type C. reinhardtii nit1 gene (encodes nitrate reductase) as selectable markers (p5' delta and p3' delta respectively) and the low reverting nit1-305 strain as the transformation recipient. After introduction of the DNA into the cell, intermolecular recombination between p5' delta and p3' delta occurs at a high frequency to restore a functional nit1 gene, indicating the presence of homologous recombination machinery in mitotic cells. Gene-targeting events at the nit1 locus were selected by restoring nit1-305 cells to prototrophy after transformation with only p5' delta and were confirmed by analysis of genomic DNA. By comparing the number of transformants obtained after transformation with p5' delta to the number obtained after transformation with a functional nit1 gene, the frequency of homologous-to-random integration events ranged between 1:1000 after glass bead-mediated transformation and 1:24 after bombardment with DNA-coated tungsten microprojectiles.

摘要

到目前为止,单细胞绿藻莱茵衣藻的核转化特征是将导入的DNA整合到非同源位点。在本研究中,为了开发基因靶向和基因破坏策略,对转化过程中同源重组事件的发生情况进行了研究。通过使用野生型莱茵衣藻nit1基因(编码硝酸还原酶)的无功能5'和3'缺失衍生物作为选择标记(分别为p5'δ和p3'δ)以及低回复率的nit1 - 305菌株作为转化受体来监测同源重组。将DNA导入细胞后,p5'δ和p3'δ之间的分子间重组高频发生,以恢复功能性nit1基因,这表明有丝分裂细胞中存在同源重组机制。通过仅用p5'δ转化后将nit1 - 305细胞恢复为原养型来选择nit1位点的基因靶向事件,并通过基因组DNA分析进行确认。通过比较用p5'δ转化后获得的转化体数量与用功能性nit1基因转化后获得的转化体数量,同源整合与随机整合事件的频率在玻璃珠介导的转化后为1:1000,在用包被DNA的钨微弹轰击后为1:24。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/837314b592c7/pnas01476-0453-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/387730191a29/pnas01476-0452-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/22e3128cfac9/pnas01476-0452-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/16ae85326b4d/pnas01476-0452-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/837314b592c7/pnas01476-0453-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/387730191a29/pnas01476-0452-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/22e3128cfac9/pnas01476-0452-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/16ae85326b4d/pnas01476-0452-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a72/47530/837314b592c7/pnas01476-0453-a.jpg

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