Delanversin G, Jacq B
C R Seances Acad Sci III. 1983;296(22):1041-4.
A 431 nucleotide sequence from the central break region of Drosophila 26S rRNA precursor has been established by sequencing the corresponding region of the 26S gene. The analysis of rDNA-mature 26S rRNA hybrids submitted to S1 nuclease digestion has allowed us to show that a 75 +/- 3 nucleotide A-U rich RNA fragment is excised during the processing of the precursor.
通过对果蝇26S基因相应区域进行测序,已确定了来自果蝇26S rRNA前体中央断裂区域的一段431个核苷酸的序列。对经S1核酸酶消化的rDNA - 成熟26S rRNA杂交体的分析使我们能够表明,在前体加工过程中会切除一个75±3个核苷酸的富含A - U的RNA片段。