Hueros G, Varotto S, Salamini F, Thompson R D
Max-Planck-Institut für Züchtungsforschung, Cologne, Germany.
Plant Cell. 1995 Jun;7(6):747-57. doi: 10.1105/tpc.7.6.747.
A cDNA clone, BET1 (for basal endosperm transfer layer), was isolated from a cDNA bank prepared from 10-days after pollination (DAP) maize endosperm mRNA. BET1 mRNA was shown to encode a 7-kD cell wall polypeptide. Both the mRNA and protein were restricted in their distribution to the basal endosperm transfer layer and were not expressed elsewhere in the plant. BET1 expression commenced at 9 DAP, reached a maximum between 12 and 16 DAP, and declined after 16 DAP. The initial accumulation of the BET1 polypeptide reached a plateau by 16 DAP and declined thereafter, becoming undetectable by 20 DAP. The antibody raised against the BET1 protein reacted with a number of polypeptides of higher molecular mass than the BET1 monomer. Most of these were present in cytosolic fractions and were found in nonbasal cell endosperm extracts, but three species appeared to be basal cell specific. This result and the reactivity of exhaustively extracted cell wall material with the BET1 antibody suggest that a fraction of the protein is deposited in a covalently bound form in the extracellular matrix. We propose that the BET1 protein plays a role in the structural specialization of the transfer cells. In addition, BET1 provides a new molecular marker for the development of this endosperm domain.
从授粉后10天(DAP)的玉米胚乳mRNA制备的cDNA文库中分离出一个cDNA克隆,即BET1(基础胚乳转移层)。研究表明,BET1 mRNA编码一种7-kD的细胞壁多肽。mRNA和蛋白质的分布都局限于基础胚乳转移层,在植物的其他部位不表达。BET1的表达在9 DAP开始,在12至16 DAP之间达到最大值,16 DAP后下降。BET1多肽的初始积累在16 DAP时达到平台期,此后下降,到20 DAP时无法检测到。针对BET1蛋白产生的抗体与一些分子量高于BET1单体的多肽发生反应。其中大多数存在于胞质组分中,在非基础细胞胚乳提取物中也能找到,但有三种似乎是基础细胞特异性的。这一结果以及用BET1抗体对彻底提取的细胞壁材料的反应表明,一部分蛋白质以共价结合的形式沉积在细胞外基质中。我们认为BET1蛋白在转移细胞的结构特化中起作用。此外,BET1为该胚乳区域的发育提供了一个新的分子标记。