Biomedical Engineering Reference
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Watson-crick base pairing with an antisense oligonucleotide. This would presumably
greatly simplify the development of generic delivery systems with the appropriate
pharmacokinetics since the only difference between imaging agents would be the
precise sequence of the antisense agent for a given nucleic acid target. Nucleic acids
have already been extensively exploited for ex vivo diagnostic applications, and
many disease-specific target sequences are known [16-19]. Potential nucleic acid
targets within a cell are duplex DNA residing within the nucleus and in the mitochon-
dria and various RNAs that are transcribed from the DNA such as messenger RNA
(mRNA), ribosomal RNA (rRNA), and noncoding RNAs such as microRNAs
(miRNAs) (Fig. 13.2).
Chromosomal DNA
snoRNA
tRNA
snoRNA + rRNA
lncRNA
rRNA
snoRNA
Nucleolus
rRNA
snoRNA
Pre-mRNA
Pri-miRNA
Cap
AAAA
Cap
AAAA
snRNP
Splicing
Nucleus
Cytoplasm
snRNA
Pre-mirna
Dicer
Cap
AAAA
miRNA
duplex
rRNA
Translation
tRNA
rRNA
RISC
complex
Protein
fIgure 13.2 Potential nucleic acid targets for genetic imaging agents. Shown are some of
the major nucleic acid metabolism pathways in the nucleus and cytoplasm of a cell. Not shown
are targets in the mitochondrion that contains mtDNA, which encodes its own rRNA, mRNAs,
tRNAs, and ncRNAs.
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