In vitro octaploid induction of Populus hopeiensis with colchicine.

Colchicine Octaploid Phenotypic variation Populus hopeiensis Stomata

Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
06 Apr 2022
Historique:
received: 12 02 2022
accepted: 31 03 2022
entrez: 7 4 2022
pubmed: 8 4 2022
medline: 9 4 2022
Statut: epublish

Résumé

Autopolyploids, especially artificial lines, provide model systems for understanding the mechanisms of gene dosage effects on trait variation owing to their relatively uniform genetic background. Here, a protocol for in vitro octaploid induction of Populus hopeiensis from leaf blades with colchicine treatment was established through investigation of the effects of different pre-culture durations, colchicine concentrations, and exposure times. We found that pre-culture duration, colchicine concentration, and exposure time had significant effects on the survival rate, shoot regeneration rate, and octaploid induction rate of P. hopeiensis leaf blades. The highest octaploid induction rate (8.61%) was observed when leaf blades pre-cultured for 9 days were treated for 4 days with 100 μM colchicine. The ploidy level of all regenerated plantlets was analyzed by flow cytometry and further confirmed by chromosome counting. A total of 14 octaploids were obtained. The stomatal length, width, and density of leaf blades significantly differed between tetraploid and octaploid plants. Compared with diploid and tetraploid plants, octaploids had a slower growth rate, smaller leaf blade size, and shorter internodes. We established an effective protocol for inducing octaploids in vitro from autotetraploid P. hopeiensis leaf blades by colchicine treatment.

Sections du résumé

BACKGROUND BACKGROUND
Autopolyploids, especially artificial lines, provide model systems for understanding the mechanisms of gene dosage effects on trait variation owing to their relatively uniform genetic background. Here, a protocol for in vitro octaploid induction of Populus hopeiensis from leaf blades with colchicine treatment was established through investigation of the effects of different pre-culture durations, colchicine concentrations, and exposure times.
RESULTS RESULTS
We found that pre-culture duration, colchicine concentration, and exposure time had significant effects on the survival rate, shoot regeneration rate, and octaploid induction rate of P. hopeiensis leaf blades. The highest octaploid induction rate (8.61%) was observed when leaf blades pre-cultured for 9 days were treated for 4 days with 100 μM colchicine. The ploidy level of all regenerated plantlets was analyzed by flow cytometry and further confirmed by chromosome counting. A total of 14 octaploids were obtained. The stomatal length, width, and density of leaf blades significantly differed between tetraploid and octaploid plants. Compared with diploid and tetraploid plants, octaploids had a slower growth rate, smaller leaf blade size, and shorter internodes.
CONCLUSIONS CONCLUSIONS
We established an effective protocol for inducing octaploids in vitro from autotetraploid P. hopeiensis leaf blades by colchicine treatment.

Identifiants

pubmed: 35387617
doi: 10.1186/s12870-022-03571-3
pii: 10.1186/s12870-022-03571-3
pmc: PMC8985302
doi:

Substances chimiques

Colchicine SML2Y3J35T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

176

Informations de copyright

© 2022. The Author(s).

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Auteurs

Jian Wu (J)

National Engineering Laboratory for Tree Breeding, Beijing Forestry University, Beijing, 100083, China.
Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, Beijing Forestry University, Beijing, 100083, China.
College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China.

Xuetong Cheng (X)

National Engineering Laboratory for Tree Breeding, Beijing Forestry University, Beijing, 100083, China.
Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, Beijing Forestry University, Beijing, 100083, China.
College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China.

Bo Kong (B)

National Engineering Laboratory for Tree Breeding, Beijing Forestry University, Beijing, 100083, China.
Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, Beijing Forestry University, Beijing, 100083, China.
College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China.

Qing Zhou (Q)

National Engineering Laboratory for Tree Breeding, Beijing Forestry University, Beijing, 100083, China.
Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, Beijing Forestry University, Beijing, 100083, China.
College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China.

Yaru Sang (Y)

National Engineering Laboratory for Tree Breeding, Beijing Forestry University, Beijing, 100083, China.
Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, Beijing Forestry University, Beijing, 100083, China.
College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China.

Pingdong Zhang (P)

National Engineering Laboratory for Tree Breeding, Beijing Forestry University, Beijing, 100083, China. zhangpd@bjfu.edu.cn.
Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, Beijing Forestry University, Beijing, 100083, China. zhangpd@bjfu.edu.cn.
College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China. zhangpd@bjfu.edu.cn.

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Classifications MeSH