【摘 要】
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A novel pollen-specific full-length eDNA clone PSG076 was isolated using suppression single gene based on different poly(A) tail attachment sites. However, poly
【机 构】
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Institute of Biochemistry, Zhejiang University, Hangzhou 310029, China
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A novel pollen-specific full-length eDNA clone PSG076 was isolated using suppression single gene based on different poly(A) tail attachment sites. However, polyadenylation consensus sequence and an open reading frame of 663 bp encoding a 221 amino acid peptide with pI of 4.31. A blast search revealed that this sequence did not show a significant similarity to any genes deposited in the public database.Southe blot indicated that PSG076 was a single copy gene. Northe blot and RT-PCR analysis indicated that PSG076 transcripts showed specific expression in mature pollen, and weak or undetectable signals in uninucleate microspore, immature seed, stem, young leave, root and ovary. Further analysis of the expression patte in gametophyte showed that PSG076 transcripts were undetectable in uninucleate, binucleate microspore and pollen at early stage, and were first detectable and increased rapidly at middle and late stages of pollen development with the maximum level in mature pollen and also expressed in germinating pollen in vivo, suggesting that PSG076might play a role in pollen germination and pollen tube growth in addition to its function in maturation. The evidences gathered in this work indicated that the six different transcripts from the single gene were differentially expressed during pollen development.
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