Magnard Jean-Louis, Lehouque Gaëlle, Massonneau Agnès, Frangne Nathalie, Heckel Thierry, Gutierrez-Marcos José F, Perez Pascual, Dumas Christian, Rogowsky Peter M
RDP, UMR 5667 INRA-CNRS-ENSL-UCBL, ENS-Lyon, 46 Allée d'Italie, 69364 Lyon Cedex 07, France.
Plant Mol Biol. 2003 Dec;53(6):821-36. doi: 10.1023/B:PLAN.0000023672.37089.00.
Two novel maize genes expressed specifically in the central cell of the female gametophyte and in two compartments of the endosperm (the basal endosperm transfer layer and the embryo surrounding region) were characterized. The ZmEBE (embryo sac/basal endosperm transfer layer/embryo surrounding region) genes were isolated by a differential display between the upper and the lower half of the kernel at 7 days after pollination (DAP). Sequence analysis revealed ORFs coding for two closely related proteins of 304 amino acids (ZmEBE-1) and 286 amino acids (ZmEBE-2). This size difference was due to differences in the splicing of the two genes. Both protein sequences showed significant similarity to the DUF239 family of Arabidopsis, a group of 22 proteins of unknown function, a small number of which are putative peptidases. ZmEBE genes had a novel cell type-specific expression pattern in the central cell before and the resulting endosperm after fertilization. RT-PCR analysis showed that the expression of both genes started before pollination in the central cell and continued in the kernel up to 20 DAP with a peak at 7 DAP. In situ hybridization revealed that the expression in the kernel was restricted to the basal transfer cell layer and the embryo surrounding region of the endosperm. The expression of ZmEBE-1 was at least 10 times lower than that of ZmEBE-2. Similarly to other genes expressed in the endosperm, ZmEBE-1 expression was subject to a parent-of-origin effect, while no such effect was detected in ZmEBE-2. Sequence analysis of upstream regions revealed a potential cis element of 33 bp repeated 7 times in ZmEBE-1 and ZmEBE-2 between positions -900 and -100. The 1.6 kb ZmEBE-2 upstream sequence containing the seven R7 elements was able to confer expression in the basal endosperm to a Gus reporter gene. These data indicate that ZmEBE is potentially involved in the early development of specialized domains of the endosperm and that this process is possibly already initiated in the central cell, which is at the origin of the endosperm.
对两个新的玉米基因进行了表征,它们在雌配子体的中央细胞以及胚乳的两个区域(胚乳基部转移层和胚周区)中特异性表达。通过授粉后7天(DAP)玉米粒上下半部分之间的差异显示分离出ZmEBE(胚囊/胚乳基部转移层/胚周区)基因。序列分析揭示了编码两个密切相关蛋白质的开放阅读框,一个含304个氨基酸(ZmEBE - 1),另一个含286个氨基酸(ZmEBE - 2)。这种大小差异是由于两个基因剪接的不同。两个蛋白质序列与拟南芥的DUF239家族显示出显著相似性,该家族有22个功能未知的蛋白质,其中少数是假定的肽酶。ZmEBE基因在受精前的中央细胞以及受精后形成的胚乳中具有新的细胞类型特异性表达模式。RT - PCR分析表明,两个基因的表达在授粉前在中央细胞中开始,并在玉米粒中持续到20 DAP,在7 DAP时达到峰值。原位杂交显示,玉米粒中的表达仅限于胚乳基部转移细胞层和胚周区。ZmEBE - 1的表达比ZmEBE - 2至少低10倍。与其他在胚乳中表达的基因类似,ZmEBE - 1的表达受亲本来源效应的影响,而在ZmEBE - 2中未检测到这种效应。上游区域的序列分析揭示了一个33 bp的潜在顺式元件,在ZmEBE - 1和ZmEBE - 2中,在 - 900和 - 100位置之间重复7次。包含七个R7元件的1.6 kb ZmEBE - 2上游序列能够使Gus报告基因在胚乳基部表达。这些数据表明,ZmEBE可能参与胚乳特定区域的早期发育,并且这个过程可能已经在作为胚乳起源的中央细胞中启动。