Xu Jian-Hong, Messing Joachim
Waksman Institute of Microbiology, Rutgers University, Piscataway, NJ 08854, USA.
BMC Genet. 2006 Nov 9;7:52. doi: 10.1186/1471-2156-7-52.
Genetic maps are based on recombination of orthologous gene sequences between different strains of the same species. Therefore, it was unexpected to find extensive non-collinearity of genes between different inbred strains of maize. Interestingly, disruption of gene collinearity can be caused among others by a rolling circle-type copy and paste mechanism facilitated by Helitrons. However, understanding the role of this type of gene amplification has been hampered by the lack of finding intact gene sequences within Helitrons.
By aligning two haplotypes of the z1C1 locus of maize we found a Helitron that contains two genes, one encoding a putative cytidine deaminase and one a hypothetical protein with part of a 40S ribosomal protein. The cytidine deaminase gene, called ZmCDA3, has been copied from the ZmCDA1 gene on maize chromosome 7 about 4.5 million years ago (mya) after maize was formed by whole-genome duplication from two progenitors. Inbred lines contain gene copies of both progenitors, the ZmCDA1 and ZmCDA2 genes. Both genes diverged when the progenitors of maize split and are derived from the same progenitor as the rice OsCDA1 gene. The ZmCDA1 and ZmCDA2 genes are both transcribed in leaf and seed tissue, but transcripts of the paralogous ZmCDA3 gene have not been found yet. Based on their protein structure the maize CDA genes encode a nucleoside deaminase that is found in bacterial systems and is distinct from the mammalian RNA and/or DNA modifying enzymes.
The conservation of a paralogous gene sequence encoding a cytidine deaminase gene over 4.5 million years suggests that Helitrons could add functional gene sequences to new chromosomal positions and thereby create new haplotypes. However, the function of such paralogous gene copies cannot be essential because they are not present in all maize strains. However, it is interesting to note that maize hybrids can outperform their inbred parents. Therefore, certain haplotypes may function only in combination with other haplotypes or under specialized environmental conditions.
遗传图谱基于同一物种不同品系间直系同源基因序列的重组。因此,在玉米不同自交系间发现广泛的基因非共线性令人意外。有趣的是,基因共线性的破坏可能由多种因素导致,其中包括由Helitrons促成的滚环式复制粘贴机制。然而,由于在Helitrons内未找到完整的基因序列,对这种基因扩增类型作用的理解受到了阻碍。
通过比对玉米z1C1位点的两个单倍型,我们发现一个Helitron包含两个基因,一个编码假定的胞苷脱氨酶,另一个编码具有40S核糖体蛋白部分序列的假定蛋白。这个胞苷脱氨酶基因名为ZmCDA3,约在450万年前(百万年前)从玉米7号染色体上的ZmCDA1基因复制而来,当时玉米由两个祖先通过全基因组复制形成。自交系包含两个祖先的基因拷贝,即ZmCDA1和ZmCDA2基因。当玉米的祖先分裂时,这两个基因发生了分化,并且与水稻的OsCDA1基因来自同一个祖先。ZmCDA1和ZmCDA2基因在叶片和种子组织中均有转录,但尚未发现旁系同源的ZmCDA3基因的转录本。基于它们的蛋白质结构,玉米CDA基因编码一种在细菌系统中发现的核苷脱氨酶,与哺乳动物的RNA和/或DNA修饰酶不同。
超过450万年里编码胞苷脱氨酶基因的旁系同源基因序列的保守性表明,Helitrons可以将功能性基因序列添加到新的染色体位置,从而创造新的单倍型。然而,这种旁系同源基因拷贝的功能并非必不可少,因为它们并非存在于所有玉米品系中。然而,值得注意的是玉米杂交种的表现可能优于其自交亲本。因此,某些单倍型可能仅在与其他单倍型组合或在特定环境条件下发挥作用。