Slabas A R, Fordham-Skelton A P, Fletcher D, Martinez-Rivas J M, Swinhoe R, Croy R R, Evans I M
Department of Biological Sciences, University of Durham, UK.
Plant Mol Biol. 1994 Nov;26(4):1125-38. doi: 10.1007/BF00040694.
Two cDNA species encoding sequences homologous to the 65 kDa regulatory subunit (PR 65) of protein phosphatase 2A (PP2A) have been isolated from an Arabidopsis thaliana cDNA library. These were designated pDF1 and pDF2. pDF1 is 1795 bp long and by comparison with the human and porcine PP2A regulatory subunit sequences represents a full-length clone. It encodes a predicted polypeptide of 587 amino acid residues. pDF2 is truncated at the 5' end by 237 bp. The complete nucleotide sequences have been determined for both cDNA species. Comparison of the nucleotide and the deduced amino acid sequences showed that the two sequences were homologous but not identical and therefore must be derived from two different genes. Northern blot analysis was performed on total RNA and poly(A)+ RNA isolated from seed at various stages of development and from young leaf material of Brassica napus L. (oilseed rape). Both cDNA probes hybridised to a single major mRNA species of ca. 2.2 kb. The highest level of expression was observed in the total RNA from developing rape seed at about 33 days after flowering, and the transcript level in the poly(A)+ RNA of the seed was higher than in young leaf of oilseed rape. Southern blot analysis was performed on two varieties of A. thaliana and B. napus genomic DNA; this identified a small family of genes in A. thaliana consisting of at least 2 or 3 members and a larger multigene family in B. napus of at least 5 or 6 members. Two independent genomic clones were isolated from an A. thaliana genomic library. Sequencing of a fragment common to both revealed that the sequence was identical in both clones and, therefore, they were assumed to contain the same genomic sequence. The genomic sequence selected, designated regA, is 3639 bp long and the coding sequence contains eleven introns. The gene encodes a predicted polypeptide of 590 amino acid residues. The sequence comparison with both cDNA sequences showed that it is homologous but not identical to the two, confirming that at least three different genes exist in A. thaliana which encode PR65 of PP2A.
已从拟南芥cDNA文库中分离出两种编码与蛋白磷酸酶2A(PP2A)65 kDa调节亚基(PR 65)同源序列的cDNA。它们被命名为pDF1和pDF2。pDF1长1795 bp,与人和猪的PP2A调节亚基序列相比,代表一个全长克隆。它编码一个预测的由587个氨基酸残基组成的多肽。pDF2在5'端截短了237 bp。已确定了这两种cDNA的完整核苷酸序列。核苷酸和推导的氨基酸序列比较表明,这两个序列同源但不相同,因此必定来自两个不同的基因。对从不同发育阶段的种子以及甘蓝型油菜(油菜)幼叶材料中分离的总RNA和聚腺苷酸加尾RNA(poly(A)+ RNA)进行了Northern印迹分析。两种cDNA探针均与一条约2.2 kb的主要mRNA杂交。在开花后约33天发育中的油菜种子的总RNA中观察到最高表达水平,并且种子的聚腺苷酸加尾RNA中的转录本水平高于油菜幼叶中的水平。对两种拟南芥和甘蓝型油菜基因组DNA进行了Southern印迹分析;这确定了拟南芥中的一个小基因家族,至少由2或3个成员组成,以及甘蓝型油菜中的一个更大的多基因家族,至少由5或6个成员组成。从拟南芥基因组文库中分离出两个独立的基因组克隆。对两者共有的一个片段进行测序表明,该序列在两个克隆中相同,因此,假定它们包含相同的基因组序列。所选的基因组序列命名为regA,长3639 bp,编码序列包含11个内含子。该基因编码一个预测的由590个氨基酸残基组成的多肽。与两个cDNA序列的序列比较表明,它与两者同源但不相同,证实拟南芥中至少存在三个不同的基因编码PP2A的PR65。