4.4 Article

A Simple Protocol for Thallus Culture-Based Genetic Transformation of the Liverwort Marchantia polymorpha

期刊

JOURNAL OF PLANT BIOLOGY
卷 65, 期 1, 页码 11-19

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s12374-021-09339-w

关键词

Thallus culture; Genetic transformation; Agrobacterium; Liverwort; Marchantia polymorpha

资金

  1. National Research Foundation (NRF) - Ministry of Education, South Korea [2018R1A6A1A03025607]
  2. Yonsei University Research Fund [2020-22-0083, 2020-12-0025]
  3. Young Scientist Grants Program [NRF-2020R1C1C1014389]
  4. National Research Foundation of Korea [2018R1A6A1A03025607] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The liverwort Marchantia polymorpha is a crucial model plant for molecular evolution studies, with the capability to undergo genetic transformation using different stages of thalli. The establishment of mature thalli pre-cultivation method and young thalli direct co-culture method with stable transformation efficiency provides a more efficient approach for genetic manipulation in liverworts. The focus was mainly on reducing hands-on labor time for genetic transformation procedures.
The liverwort Marchantia polymorpha, as the earliest land plant, is an important model system for studies of molecular evolution. Liverworts, which undergo a haplo-diplontic life cycle, spend most of their life as haploid gametophyte bodies, called thalli. In addition, the thalli can produce vegetative propagules, termed gemmae, conferring asexual reproduction in liverworts. Thus, to obtain sufficient isogenic tissues for genetic manipulation, the thallus is a suitable material. Here, we found that 23- to 25-d-old fully expanded thalli can be used for the genetic transformation with the pre-cultivation process, setting up the mature thalli pre-cultivation method. Next, we elucidated that 10- to 12-d-old young thalli can be used for the tissue-culture-based transformation in the absence of the pre-cultivation step, establishing the young thalli direct co-culture method without significant changes of transformation efficiency compared with the mature thalli pre-culture method. Overall, we set up the protocol using various stages of thalli of M. polymorpha with stable transformation efficiency. Mainly, we focused on reducing the hands-on labor time for performing the genetic transformation by widening the available stage of thalli for transformation or excluding the regenerating process of the thallus plantlets. In this report, we describe the detailed procedures employed under experimental conditions.

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