Biology Department, Georgia Southern University, P.O. Box 8042, Statesboro, GA 30460, USA.
Int J Mol Sci. 2024 Feb 7;25(4):2028. doi: 10.3390/ijms25042028.
Various attempts to amplify an AQP11 cDNA from tissues of the spiny dogfish () were made. Two pairs of deoxy-inosine-containing degenerate primers were designed based on conserved amino acid sequences from an AQP11 alignment. These primers yielded some faint bands from gill cDNA that were sequenced. Blast searches with the sequences showed they were not AQP11. An elasmobranch AQP11 nucleotide sequence alignment was produced to identify conserved regions to make further degenerate primers. One primer pair produced a short 148 bp fragment showing particularly strong amplification in gill and intestine. It was sequenced and represented a piece of the AQP11 gene. However, as the fragment may have resulted from contaminating genomic DNA (in total RNA used to make cDNA), 5' and 3' RACE were performed to amplify the two ends of the putative cDNA. Furthermore, 5' and 3' RACE amplifications depend on the presence of a 5' cap nucleotide and a poly A tail, respectively on the putative AQP11 mRNA. Hence, successful amplification was only possible from cDNA and not genomic DNA. Nested RACE amplifications were performed using gill and intestinal RACE cDNA, but none of the DNA fragments sequenced were AQP11. Consequently, the spiny dogfish AQP11 gene may represent a pseudogene.
我们尝试从棘鲨组织中扩增水通道蛋白 11 (AQP11) cDNA,为此设计了两对基于 AQP11 氨基酸序列比对的保守区设计了含脱氧次黄嘌呤的简并引物。这些引物从鳃 cDNA 中产生了一些微弱的条带并进行了测序。序列的 Blast 搜索表明它们不是 AQP11。为了进一步设计简并引物,我们制作了一个鲛类 AQP11 核苷酸序列比对图,以确定保守区。一对引物产生了一个特别在鳃和肠中强烈扩增的 148bp 短片段。对其进行测序,发现它代表了 AQP11 基因的一部分。然而,由于该片段可能来自污染的基因组 DNA(用于制备 cDNA 的总 RNA),因此进行了 5' 和 3' RACE 以扩增假定 cDNA 的两个末端。此外,5' 和 3' RACE 扩增分别取决于假定的 AQP11 mRNA 上 5' 帽核苷酸和多 A 尾的存在。因此,只有从 cDNA 而不是基因组 DNA 进行成功扩增。使用鳃和肠的 RACE cDNA 进行了嵌套 RACE 扩增,但测序的 DNA 片段均不是 AQP11。因此,棘鲨 AQP11 基因可能代表一个假基因。