Taylor Scott A, Hofer Julie M I, Murfet Ian C, Sollinger John D, Singer Susan R, Knox Maggie R, Ellis T H Noel
School of Plant Science, University of Tasmania, G.P.O. Box 252-55, Hobart, Tasmania, 7001, Australia.
Plant Physiol. 2002 Jul;129(3):1150-9. doi: 10.1104/pp.001677.
SQUAMOSA and APETALA1 are floral meristem identity genes from snapdragon (Antirrhinum majus) and Arabidopsis, respectively. Here, we characterize the floral meristem identity mutation proliferating inflorescence meristem (pim) from pea (Pisum sativum) and show that it corresponds to a defect in the PEAM4 gene, a homolog of SQUAMOSA and APETALA1. The PEAM4 coding region was deleted in the pim-1 allele, and this deletion cosegregated with the pim-1 mutant phenotype. The pim-2 allele carried a nucleotide substitution at a predicted 5' splice site that resulted in mis-splicing of pim-2 mRNA. PCR products corresponding to unspliced and exon-skipped mRNA species were observed. The pim-1 and pim-2 mutations delayed floral meristem specification and altered floral morphology significantly but had no observable effect on vegetative development. These floral-specific mutant phenotypes and the restriction of PIM gene expression to flowers contrast with other known floral meristem genes in pea that additionally affect vegetative development. The identification of PIM provides an opportunity to compare pathways to flowering in species with different inflorescence architectures.
SQUAMOSA和APETALA1分别是来自金鱼草(Antirrhinum majus)和拟南芥的花分生组织特征基因。在此,我们对豌豆(Pisum sativum)中花分生组织特征突变体——增殖花序分生组织(pim)进行了表征,并表明它对应于PEAM4基因的缺陷,该基因是SQUAMOSA和APETALA1的同源基因。在pim - 1等位基因中,PEAM4编码区被删除,且这种缺失与pim - 1突变体表型共分离。pim - 2等位基因在预测的5'剪接位点发生了核苷酸替换,导致pim - 2 mRNA剪接错误。观察到了与未剪接和外显子跳跃的mRNA种类相对应的PCR产物。pim - 1和pim - 2突变延迟了花分生组织的特化,并显著改变了花的形态,但对营养生长没有可观察到的影响。这些花特异性突变体表型以及PIM基因表达仅限于花的情况,与豌豆中其他已知的花分生组织基因不同,后者还会影响营养生长。PIM的鉴定为比较具有不同花序结构的物种中开花途径提供了一个机会。