Recovery patterns, histological observations and genetic integrity in Malus shoot tips cryopreserved using droplet-vitrification and encapsulation-dehydration procedures

被引:40
作者
Li, Bai-Quan [1 ]
Feng, Chao-Hong [1 ]
Wang, Min-Rui [1 ]
Hu, Ling-Yun [1 ]
Volk, Gayle [2 ]
Wang, Qiao-Chun [1 ]
机构
[1] Northwest A&F Univ, Coll Hort, State Key Lab Crop Stress Biol Arid Areas, Yangling 712100, Shaanxi, Peoples R China
[2] ARS, USDA, Natl Ctr Genet Resources Preservat, Ft Collins, CO 80521 USA
关键词
Droplet-vitrification; Encapsulation-dehydration; Genetic stability; Histological observation; Malus; Shoot tips; APPLE; STABILITY; PRECULTURE; RESOURCES; MERISTEMS; GROWTH; CELLS; BUDS; PEAR; L;
D O I
10.1016/j.jbiotec.2015.09.030
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A droplet-vitrification procedure is described for cryopreservation of Mains shoot tips. Survival patterns, recovery types, histological observations, and genetic integrity were compared for Malus shoot tips cryopreserved using this droplet-vitrification procedure and an encapsulation-dehydration procedure that was previously reported by us. In both procedures, three types of shoot tip recovery were observed following cryopreservation: callus formation without shoot regrowth, leaf formation without shoot regrowth, and shoot regrowth. Three categories of histological observations were also identified in cross-sections of shoot tips recovered after cryopreservation using the two cryogenic procedures. In category 1, almost all of the cells (94-95%) in the apical dome (AD) were damaged or killed and only some cells (30-32%) in the leaf primordia (LPs) survived. In category 2, only a few cells (18-20%) in the AD and some cells (30-31%) in the LPs survived. In category 3, majority of the cells (60-62%) in the AD and some cells (30-33%) in the LPs survived. These data suggest that shoot regrowth is correlated to the presence of a majority of surviving cells in the AD after liquid nitrogen exposure. No polymorphic bands were detected by inter-simple sequence repeats or by random amplified polymorphic DNA assessments, and ploidy levels analyzed by flow cytometry were unchanged when plants recovered after cryoexposure were compared to controls. The droplet-vitrification procedure appears to be robust since seven genotypes representing four Malus species and one hybrid recovered shoots following cryopreservation. Mean shoot regrowth levels of these seven genotypes were 48% in the droplet-vitrification method, which were lower than those (61%) in the encapsulation-dehydration procedure reported in our previous study, suggesting the latter may be preferred for routine cryobanking applications for Malus shoot tips. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 191
页数:10
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