Sun Zhong-Ping, Wang Zhan-Bin, Xu Xiang-Ling, Li Ji-Lin
Biology Department, Harbin Normal University, Harbin 150080, China.
Yi Chuan Xue Bao. 2004 Nov;31(11):1268-74.
In the present study,Chinese Spring-Imperial (1 R-7R) wheat-rye disomic addition lines were hybridized with Chinese Spring-2C (derived from Aegilops cylindrica) disomic addition lines. The F1 hybrids were examined by mitotic and meiotic analysis. There were observed abnormal chromosome configurations. A total of 430 F2 plants were obtained by self-pollination. Chromosomes aberrations, such as translocation, deletions, isobrachial and dicentromere chromosomes, are identified in F2 individual plants by C-banding combined with fluorescent in situ hybridization (FISH). Additionally, chromosome spontaneous substitutions such as 2C substituting for wheat chromosomes 2A, 2B and 2D were also observed. The rule and frequency of chromosome aberration in F2 are the following: 22 out of 430 F2 plants (5.11%) were found involving aberration rye chromosomes. Among them, 10 plants were identified as wheat-rye chromosome translocation lines comprising 2.3%. Rye chromosome deletions comprised 12 of them (2.79%). 3 isobrachial aberrations were detected (about 0.7%), too. Most of the translocation lines are with wheat centromere, only one of them is with rye centromere. Rye chromosome aberrations occurred unevenly among homoeologous groups. There were 5 in 1R, 3 in 2R, 1 in 3R, 3 in 4R, 6 in 5R and 4 in 6R. The majority of the translocation lines are terminal translocation. 54 out of the total 430 progenies are wheat deletions,and 27 are distributed in the A group, 20 in the B group and 7 in the D group respectively. Finally,we discussed the possible cause for the uneven chromosome aberration among homoeologous groups in wheat and rye as well as the effect characteristics of 2C on wheat and rye chromosome.
在本研究中,中国春-帝国(1R-7R)小麦-黑麦二体附加系与中国春-2C(源自圆柱山羊草)二体附加系杂交。对F1杂种进行有丝分裂和减数分裂分析。观察到异常的染色体构型。通过自花授粉获得了总共430株F2植株。通过C带结合荧光原位杂交(FISH)在F2单株中鉴定出染色体畸变,如易位、缺失、等臂染色体和双着丝粒染色体。此外,还观察到染色体自发替代,如2C替代小麦染色体2A、2B和2D。F2中染色体畸变的规律和频率如下:430株F2植株中有22株(5.11%)被发现涉及黑麦染色体畸变。其中,10株被鉴定为小麦-黑麦染色体易位系,占2.3%。黑麦染色体缺失有12株(2.79%)。还检测到3例等臂畸变(约0.7%)。大多数易位系具有小麦着丝粒,只有1例具有黑麦着丝粒。黑麦染色体畸变在同源组中分布不均。1R中有5例,2R中有3例,3R中有1例,4R中有3例,5R中有6例,6R中有4例。大多数易位系为末端易位。430个后代中共有54个是小麦缺失,分别分布在A组27个、B组20个和D组7个。最后,我们讨论了小麦和黑麦同源组间染色体畸变不均的可能原因以及2C对小麦和黑麦染色体的影响特征。