Jauhar Prem P
United States Department of Agriculture-Agricultural Research Service, Northern Crop Science Laboratory, Fargo, ND 58105-5677, USA.
J Hered. 2007 Mar-Apr;98(2):188-93. doi: 10.1093/jhered/esm011. Epub 2007 Apr 8.
Polyploidy is well recognized as a major force in plant speciation. Among the polyploids in nature, allopolyploids are preponderant and include important crop plants like bread wheat, Triticum aestivum L. (2n = 6x = 42; AABBDD genomes). Allopolyploidy must result through concomitant or sequential events that entail interspecific or intergeneric hybridization and chromosome doubling in the resultant hybrids. To gain insight into the mechanism of evolution of wheat, we extracted polyhaploids of 2 cultivars, Chinese Spring (CS) and Fukuhokomugi (Fuko), of bread wheat by crossing them with maize, Zea mays L. ssp. mays. The derived Ph1-polyhaploids (2n = 3x = 21; ABD) showed during meiosis mostly univalents, which produced first-division restitution (FDR) nuclei that in turn gave rise to unreduced (2n) male gametes with 21 chromosomes. The haploids on maturity set some viable seed. The mean number of seeds per spike was 1.45 +/- 0.161 in CS and 2.3 +/- 0.170 in Fuko. Mitotic chromosome preparations from root tips of the derived plantlets revealed 2n = 42 chromosomes, that is, twice that of the parental polyhaploid, which indicated that they arose by fusion of unreduced male and female gametes formed by the polyhaploid. The Ph1-induced univalency must have produced 2n gametes and hence bilateral sexual polyploidization and reconstitution of disomic bread wheat. These findings highlight the quantum jump by which bread wheat evolved from durum wheat in nature. Thus, bread wheat offers an excellent example of rapid evolution by allopolyploidy. In the induced polyhaploids (ABD) that are equivalent of amphihaploids, meiotic phenomena such as FDR led to regeneration of parental bread wheat, perhaps a simulation of the evolutionary steps that occurred in nature at the time of the origin of hexaploid wheat.
多倍体被公认为是植物物种形成中的一股主要力量。在自然界的多倍体中,异源多倍体占优势,包括重要的农作物,如面包小麦,即普通小麦(Triticum aestivum L.,2n = 6x = 42;AABBDD基因组)。异源多倍体必定是通过伴随发生或相继发生的事件产生的,这些事件需要种间或属间杂交以及由此产生的杂种中的染色体加倍。为了深入了解小麦的进化机制,我们通过将两个面包小麦品种中国春(CS)和福库小麦(Fuko)与玉米(Zea mays L. ssp. mays)杂交,提取了它们的多单倍体。得到的Ph1 - 多单倍体(2n = 3x = 21;ABD)在减数分裂期间大多呈现单价体,产生了第一次分裂 restitution(FDR)核仁,进而产生了具有21条染色体的未减数(2n)雄配子。这些单倍体成熟时结出了一些可育种子。CS每个穗的种子平均数量为1.45 ± 0.161,Fuko为2.3 ± 0.170。从衍生幼苗的根尖制备的有丝分裂染色体显示有2n = 42条染色体,即亲本多单倍体的两倍,这表明它们是由多单倍体形成的未减数雄配子和雌配子融合产生的。Ph1诱导的单价体必定产生了2n配子,从而实现了双侧有性多倍体化和二体面包小麦的重建。这些发现突出了面包小麦在自然界中从硬粒小麦进化而来的巨大飞跃。因此,面包小麦是异源多倍体快速进化的一个绝佳例子。在相当于双单倍体的诱导多单倍体(ABD)中,诸如FDR等减数分裂现象导致了亲本面包小麦的再生,这或许模拟了六倍体小麦起源时自然界中发生的进化步骤。