Crossley S J, Greenland A J, Dickinson H G
Plant Science Laboratory, University of Reading, UK.
Planta. 1995;196(3):523-9. doi: 10.1007/BF00203652.
Differential screening of a meiocyte subtractive cDNA library from Lilium henryi L. has identified a group of 16 anther-specific partial cDNAs. Three of these sequences, LHM2, LHM6 and LHM7 have been further characterised. Hybridisation in situ with antisense riboprobes of LHM2, LHM6, and LHM7 gives a strong, clear signal which, contrary to expectations, is localised to the tapetal layer surrounding the meiocytes and not the meiocytes themselves. Developmental slot blots demonstrate that mRNAs corresponding to the three LHM cDNAs are transcribed from prophase of meiosis I to the uninucleate microspore stage, while Northern analysis reveals these tapetally expressed cDNAs to correspond with transcripts of some 500 bp. Although LHM2 is less abundant than LHM6 and LHM7, the pattern of developmental expression, and the size range of the transcripts suggests that all three cDNAs may be related. The deduced polypeptide products of LHM6 and LHM7 share 71% identity over a conserved region of 38 residues. Inverse polymerase chain reaction was used to obtain the full sequence for LHM7. Its deduced protein sequence has a signal peptide indicating it may be secreted; the cleaved protein has a molecular weight of 8.9 kDa. Furthermore, the LHM7 protein has significant levels of homology with tapetally expressed proteins from Arabidopsis thaliana, Antirrhinum majus and Lycopersicon esculentum. All contain a highly conserved pattern of cysteine residues present in seed and non-specific lipid transfer proteins. The function of this gene product is discussed in the perspective of current models of another development.
对湖北百合减数分裂细胞消减cDNA文库进行差异筛选,鉴定出一组16个花药特异的部分cDNA。其中3个序列,即LHM2、LHM6和LHM7已得到进一步表征。用LHM2、LHM6和LHM7的反义核糖探针进行原位杂交,得到一个强烈、清晰的信号,与预期相反,该信号定位于围绕减数分裂细胞的绒毡层,而非减数分裂细胞本身。发育狭线印迹表明,与3个LHM cDNA对应的mRNA从减数分裂I前期转录至单核小孢子阶段,而Northern分析显示这些在绒毡层表达的cDNA与约500 bp的转录本相对应。尽管LHM2的丰度低于LHM6和LHM7,但其发育表达模式以及转录本的大小范围表明所有这3个cDNA可能相关。LHM6和LHM7推导的多肽产物在38个残基的保守区域内具有71%的同一性。采用反向聚合酶链反应获得LHM7的全长序列。其推导的蛋白质序列含有一个信号肽,表明它可能被分泌;切割后的蛋白质分子量为8.9 kDa。此外,LHM7蛋白与拟南芥、金鱼草和番茄中绒毡层表达的蛋白具有显著的同源性。所有这些蛋白都含有种子和非特异性脂质转移蛋白中存在的高度保守的半胱氨酸残基模式。从花药发育的当前模型角度讨论了该基因产物的功能。