ArticlePlant & cell physiology2016
Cryopreservation of Gemmae from the Liverwort Marchantia polymorpha L.
Article in Plant & cell physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
9 citing papers in PubMed.
- Selection of a histidine auxotrophicPlant biotechnology (Tokyo, Japan) · 2022Article
- The renaissance and enlightenment of Marchantia as a model system.The Plant cell · 2022Article
- Culture-based preservation ofPlant biotechnology (Tokyo, Japan) · 2021Article
- The unique bryophyte-specific repeat-containing protein SHORT-LEAF regulates gametophore development in moss.Plant physiology · 2021Article
- Lipid Remodeling Confers Osmotic Stress Tolerance to Embryogenic Cells during Cryopreservation.International journal of molecular sciences · 2021Article
- Article
- A gain-of-function T-DNA insertion mutant ofPlant biotechnology (Tokyo, Japan) · 2019Article
- Cryopreservation of Marchantia polymorpha spermatozoa.Journal of plant research · 2018Article
- Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The liverwort Marchantia polymorpha L. is one of the key model plants in evo-devo studies, and an increasing number of transgenic and mutant lines have been established. For reliable long-term preservation of M. polymorpha plants, spores have been used, but crossing is indispensable to obtain them. Gemmae, however, are vegetative clones and readily available in large numbers without crossing, thereby enabling the clonal preservation and rapid propagation of transgenic or mutant lines. Here, we report a simple cryopreservation protocol for in vitro grown M. polymorpha gemmae using aluminum cryoplates. Gemmae were pre-cultured on sucrose-containing medium, embedded in calcium alginate gel on the surface of a cryoplate, moderately dehydrated and stored in liquid nitrogen. After rapid thawing, the stored gemmae showed a 100% survival rate. Our protocol does not require plant growth regulators such as ABA, and takes only 1 h to complete except for 1 d of pre-culture. Furthermore, gemmae treated as described above but then air-dried for 2 h can be stored at -80°C for at least 1 year without a significant decrease in survival rate, which is convenient for most laboratories that have a -80°C freezer but not a liquid nitrogen container for long-term storage. These preservation techniques for M. polymorpha should increase their availability in the research community.
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