Liu ShaoJun, Duan Wei, Tao Min, Zhang Chun, Sun YuanDong, Shen JiaMin, Wang Jing, Luo KaiKun, Liu Yun
Key Laboratory of Protein Chemistry and Fish Developmental Biology of Education Ministry of China, College of Life Sciences, Hunan Normal University, Changsha 410081, China.
Sci China C Life Sci. 2007 Apr;50(2):186-93. doi: 10.1007/s11427-007-0032-2.
This study investigated the gynogenetic cytobiological behavior of the third gynogenetic generation (G(3)), which was generated from the diploid eggs produced by the second gynogenetic generation (G(2)) of red crucian carp x common carp, and determined the chromosomal numbers of G(3), G(2)xscatter scale carp and G(2)xallotetraploid hybrids of red crucian carp x common carp. The results showed that the diploid eggs of G(2) with 100 chromosomes, activated by UV-irradiated sperm from scatter scale carp and without the treatment for doubling the chromosomes, could develop into G(3) with 100 chromosomes. Similar to the first and second gynogenetic generations (G(1) and G(2)), G(3) was also diploid (2n=100) and presented the hybrid traits. The triploids (3n=150) and tetraploids (4n=200) were produced by crossing G(2) with scatter scale carp, and crossing G(2) with allotetraploids, respectively. The extrusion of the second polar body in the eggs of G(2) ruled out the possibility that the retention of the second polar body led to the formation of the diploid eggs. In addition, we discussed the mechanism of the formation of the diploid eggs generated by G(2). The establishment of the diploid gynogenesis clonal line (G(1), G(2) and G(3)) provided the evidence that the diploid eggs were able to develop into a new diploid hybrid clonal line by gynogenesis. By producing the diploid eggs as a unique reproductive way, the diploid gynogenetic progeny of allotetraploid hybrids of red crucian carp x common carp had important significances in both biological evolution and production application.
本研究对由红鲫×鲤第二代雌核发育子代(G(2))产生的二倍体卵子发育而来的第三代雌核发育子代(G(3))的雌核细胞生物学行为进行了研究,并测定了G(3)、G(2)×散鳞镜鲤及红鲫×鲤的G(2)×异源四倍体杂种的染色体数目。结果表明,G(2)的含100条染色体的二倍体卵子,经散鳞镜鲤紫外线照射精子激活且未进行染色体加倍处理,可发育成含100条染色体的G(3)。与第一代和第二代雌核发育子代(G(1)和G(2))相似,G(3)也是二倍体(2n = 100),并表现出杂种性状。三倍体(3n = 150)和四倍体(4n = 200)分别是通过G(2)与散鳞镜鲤杂交以及G(2)与异源四倍体杂交产生的。G(2)卵子中第二极体的排出排除了第二极体保留导致二倍体卵子形成的可能性。此外,我们还讨论了G(2)产生二倍体卵子的形成机制。二倍体雌核发育克隆系(G(1)、G(2)和G(3))的建立提供了证据,证明二倍体卵子能够通过雌核发育形成新的二倍体杂种克隆系。红鲫×鲤异源四倍体杂种的二倍体雌核发育后代以产生二倍体卵子作为独特的繁殖方式,在生物进化和生产应用方面都具有重要意义。