Chae K S, Murakawa K, Okubo K, Matsubara K
Institute for Molecular and Cellular Biology, Osaka University, Japan.
Gene. 1994 May 16;142(2):199-205. doi: 10.1016/0378-1119(94)90261-5.
For the PCR-based chromosomal assignment of very short cDNA fragments specifically designed primers are required. We tested primers with very short core sequences that are identical or complementary to known cDNA sequences, with or without tails at the 5' ends. The lower limit of the core length for PCR using human chromosome templates was 14 nucleotides (nt) when they have tails. The minimal length of the tail was 2 nt when it was attached to the 5' end of a 14-nt core. In the absence of a tail, 15 nt are needed for the core to act properly. The overall size of the short cDNA fragments that could be assigned was further reduced by using a pair of primers that overlap at the 3' ends. The limits of the free energy of overlap were about -1.9 kcal/mol at 45 degrees C, -2.9 kcal/mol at 50 degrees C and -4.5 kcal/mol at 55 degrees C. A combination of these features in a primer pair allowed cDNA fragments as short as 30 nt to be assigned.
对于基于PCR的极短cDNA片段的染色体定位,需要设计特异性引物。我们测试了具有非常短的核心序列的引物,这些核心序列与已知cDNA序列相同或互补,5'端有或没有尾巴。当使用人类染色体模板进行PCR时,有尾巴的引物核心长度下限为14个核苷酸(nt)。当尾巴连接到14 nt核心的5'端时,尾巴的最小长度为2 nt。在没有尾巴的情况下,核心需要15 nt才能正常发挥作用。通过使用一对在3'端重叠的引物,可定位的短cDNA片段的整体大小进一步减小。在45℃时重叠自由能的极限约为-1.9 kcal/mol,在50℃时约为-2.9 kcal/mol,在55℃时约为-4.5 kcal/mol。引物对中这些特征的组合使得短至30 nt的cDNA片段能够被定位。