Temasek Life Sciences Laboratory, 1 Research Link, National University of Singapore, Singapore 117604.
Nucleic Acids Res. 2011 Apr;39(8):3340-9. doi: 10.1093/nar/gkq1185. Epub 2010 Dec 10.
RNA localization is emerging as a general principle of sub-cellular protein localization and cellular organization. However, the sequence and structural requirements in many RNA localization elements remain poorly understood. Whereas transcription factor-binding sites in DNA can be recognized as short degenerate motifs, and consensus binding sites readily inferred, protein-binding sites in RNA often contain structural features, and can be difficult to infer. We previously showed that zebrafish squint/nodal-related 1 (sqt/ndr1) RNA localizes to the future dorsal side of the embryo. Interestingly, mammalian nodal RNA can also localize to dorsal when injected into zebrafish embryos, suggesting that the sequence motif(s) may be conserved, even though the fish and mammal UTRs cannot be aligned. To define potential sequence and structural features, we obtained ndr1 3'-UTR sequences from approximately 50 fishes that are closely, or distantly, related to zebrafish, for high-resolution phylogenetic footprinting. We identify conserved sequence and structural motifs within the zebrafish/carp family and catfish. We find that two novel motifs, a single-stranded AGCAC motif and a small stem-loop, are required for efficient sqt RNA localization. These findings show that comparative sequencing in the zebrafish/carp family is an efficient approach for identifying weak consensus binding sites for RNA regulatory proteins.
RNA 定位正在成为亚细胞蛋白定位和细胞组织的一般原则。然而,许多 RNA 定位元件的序列和结构要求仍知之甚少。虽然 DNA 中的转录因子结合位点可以被识别为短的简并基序,并容易推断出共识结合位点,但 RNA 中的蛋白质结合位点通常包含结构特征,并且难以推断。我们之前表明,斑马鱼斜视/节点相关 1(sqt/ndr1)RNA 定位于胚胎的未来背侧。有趣的是,当将哺乳动物节点 RNA 注射到斑马鱼胚胎中时,也可以定位到背侧,这表明即使鱼类和哺乳动物 UTR 不能对齐,序列基序(s)可能是保守的。为了定义潜在的序列和结构特征,我们从大约 50 种与斑马鱼密切相关或远缘相关的鱼类中获得了 ndr1 3'-UTR 序列,用于高分辨率系统发育足迹分析。我们在斑马鱼/鲤鱼家族和鲶鱼中鉴定出保守的序列和结构基序。我们发现,单个 AGCAC 基序和一个小茎环是有效定位 sqt RNA 所必需的两个新基序。这些发现表明,在斑马鱼/鲤鱼家族中进行比较测序是识别 RNA 调节蛋白的弱共识结合位点的有效方法。