Nevertheless, in an attempt to overcome the various nonspecific problems, new chemical modifications have been developed. 4A). Splicing occurs during the maturation step and can be inhibited by the hybridization of an oligonucleotide to the 5 and 3 regions involved in this process (62). Correction of -thalassemia mutant by base editor in human embryos. There will be important significance for the tumor exosomal escape mechanism to understand and treat cancer. Identification, purification and partial characterization of an oligonucleotide receptor in membranes of HepG2 cells. (G) Schematic of gRNA design and construction for circRHOBTB3. A. Tunable protein synthesis by transcript isoforms in human cells. Eventually the body cannot keep up with repair and regeneration, which leads to muscle loss (wasting) and weakness. Benson MD, Waddington-Cruz M, Berk JL, et al.. Inotersen treatment for patients with hereditary transthyretin amyloidosis, Dose-Dependent lowering of mutant huntingtin using antisense oligonucleotides in Huntington disease patients. In fact, compared with the 5-untranslated or initiation codon regions, there exists just a few examples of modified oligonucleotides able to induce an antisense effect when targeted to coding regions (22, 45, 69, 70). Adv. Haltenhof, T. et al. Exons whose inclusion in the mature mRNA is inhibited by slow, and promoted by fast, transcript elongation. Eng. Methods 13, 10291035 (2016). To date, endosomal sorting complex required for transport (ESCRT)-dependent and ESCRT-independent pathways have been reported to regulate exosomes to sort cargos. Because hsa_circ_0007444 consists of exons 6 and 7 of RHOBTB3, we hereafter referred to it as circRHOBTB3. Cell. In Smn1/; SMN2+/+ mice, SSOs that restore SMA2 exon 7 splicing also restored tail and ear necrosis phenotypes.65 Nusinersin was well tolerated in patients with SMA1,66,67 and was approved by the FDA for use in humans for the treatment of SMA in December of 2016.27. Mol. J Exp Clin Cancer Res. The results showed a higher circRHOBTB3 level in the serum of CRC patients than in that of healthy donors, which was consistent with the database (Fig. [10][12] Currently, the consensus is that the phenotype of spinal muscular atrophy spans a continuum of symptoms without clear delineation of subtypes. Exons whose inclusion in the mature mRNA is promoted by slow, and inhibited by fast, transcript elongation. Minikel has received funding for travel and/or speaker honoraria from Illumina and has received research support from Charles River Laboratories, NIH (F31 AI22952), and Prion Alliance. Boffa, L. C., Morris, P. L., Carpaneto, E. M., Louissaint, M., and Allfrey, V. G. Invasion of the CAG triplet repeats by a complementary peptide nucleic acid inhibits transcription of the androgen receptor and TATA-binding protein genes and correlates with refolding of an active nucleosome containing a unique AR gene sequence. [47][48] It was approved for use in the US in 2016, and for use in the EU in 2017. Biol. An official website of the United States government. Learn more Nature 569, 433437 (2019). Nucleic Acid Ther. Zhang L, Yu D. Exosomes in cancer development, metastasis, and immunity. [Google Scholar] 178. Nat. 5D), we found that deletion of the 141165 or 216240nt sequence significantly blocked exosomal secretion of circRHOBTB3 (Fig. Vaerman, J. L., Moureau, P., Deldime, F., Lewalle, P., Lammineur, C., Morschhauser, F., and Martiat, P. Antisense oligodeoxyribonucleotides suppress hematologic cell growth through stepwise release of deoxyribonucleotides. The genetic revolution led to the identification of many neurologic disease genes. Received 2018 Dec 17; Accepted 2019 Feb 14. [58][59] It is a pyridazine derivative that works by increasing the amount of functional survivor motor neuron protein produced by the SMN2 gene through modifying its splicing pattern. Scoles has received research support from the NINDS (U01NS103883 and R01NS097903) and Harrington Discovery Institute. S3E). CAS Targeted delivery of CRISPR/Cas9-mediated cancer gene therapy via liposome-templated hydrogel nanoparticles. June, C. H. & Sadelain, M. Chimeric antigen receptor therapy. Nat. Nat. [65][medical citation needed] Therein, it could be necessary in SMA type I and people with more severe type II to have a feeding tube or gastrostomy. (A) Schematic of the liver metastasis model for ASO injection construction. Nat. Targeted exon skipping with AAV-mediated split adenine base editors. Interestingly, we found that CRC cells could actively secrete more circRHOBTB3 than normal cells. This can result in trouble standing up. Blake, K. R., Murakami, A., Spitz, S. A., Glave, S. A., Reddy, M. P., Tso, P. O., and Miller, P. S. Hybridization arrest of globin synthesis in rabbit reticulocyte lysates and cells by oligodeoxyribonucleoside methylphosphonates. Med. 10, 212 (2019). 2022 BioMed Central Ltd unless otherwise stated. 208, 4453 (2015). Kornblihtt, A. R. et al. Baralle, F. E. & Giudice, J. Liu, X. et al. Oligonucleotides have been utilized for the last two decades for their therapeutic properties. Mol. Nat. E.M.P. Frac-seq reveals isoform-specific recruitment to polyribosomes. 18, 755768 (2004). 6H and S9E). Nevertheless, despite their inability to induce RNase H activity, these oligonucleotides were still potent inhibitors of ICAM-1 expression in human umbilical vein endothelial cells. ASO = antisense oligonucleotide; DMD = Duchenne muscular dystrophy; ESE = exonic splicing enhancer; ISS = intronic splicing silencer; LncRNA = long noncoding RNA; SMN = survival motor neuron. Perez-Pinera, P. et al. Liu, Y., Beyer, A. Sci. Alternative splicing rewires Hippo signaling pathway in hepatocytes to promote liver regeneration. Predicting antisense oligonucleotide inhibitory efficacy: a computational approach using histograms and thermodynamic indices. Orna will follow this up on Tuesday with a poster on its preclinical work in Duchenne Muscular Dystrophy (DMD). Transl. I.M.S. is an employee and shareholder of Beam Therapeutics. RNA targeting therapeutics: molecular mechanisms of antisense oligonucleotides as a therapeutic platform. 2020;52:75967. Rev. Biotechnol. & Blencowe, B. J. Science 361, 12591262 (2018). CC and KY performed statistical analysis. Such inhibition can lead to the lack of expression of a mature protein (42, 63) or, as numerous reports have shown, to the correction of aberrant splicing and the restoration of a functional protein (64, 65). Kurt, I. C. et al. Engineered CRISPRCas9 nucleases with altered PAM specificities. (A) The reanalyzed GEO datasets in this study. However, we could use this cis-element as an antitumor target by increasing circRHOBTB3 levels. Alternative isoform regulation in human tissue transcriptomes. Oligonucleotides target the altered messenger RNA (mRNA) and decrease the synthesis of the causative protein-Huntingtin. In the second step of splicing, the uncleaved intron 3 end is the (phosphodi)ester and the free exon is the alcohol. It is interesting to note that the only oligonucleotide currently approved is Vitravene(Novartis, New York, NY, USA), which is used for cytomegalovirus retinitis, where the drug is directly administered to the site of disease (intravitreal). 6A) targeting a negative circularization element (ASO-cir for 266290nt) and exosome secretion elements (ASO-exo1 for 141165nt and ASO-exo2 for 216240nt) to increase the intracellular level of circRHOBTB3 (Fig. 3H), which demonstrated that there were cis-elements in the 141240nt and 241340nt regions that promote or inhibit circRHOBTB3 circularization, respectively. (G) Cell proliferation and (H) quantification of migration and invasion assays of ASO-NC- and ASO-exo2-treated SW480 cells. Kidney function should be monitored in patients taking AMONDYS 45. Ethical approval was obtained from the the Ethics Committee of department of Medicine, Zhejiang University (Ethics Committee number: 2021021) and all participating patients were informed. PS ASOs are usually stereorandom with regard to chiral PS centers, each of which has 2 distinct stereochemical configurations, making 219 stereoisoforms possible for a 20mer ASO with 19 linkages. Otherwise, AluSx exhibited a stronger effect on regulating circRHOBTB3 circularization than AluY, which might be attributed to steric hindrance. Szakonyi, D. & Duque, P. Alternative splicing as a regulator of early plant development. Indeed, existing pipelines for the development of ASO therapies for spinocerebellar ataxias, Huntington disease, Alzheimer disease, amyotrophic lateral sclerosis, Parkinson disease, and others, and increased focus by the pharmaceutical industry on ASO development, strengthen the outlook for using ASOs for neurodegenerative diseases. Along with the advancement of technology, these modified ASOs have been applied to treat some diseases, such as cytomegalovirus (CMV)-induced chorioretinitis, Duchenne muscular dystrophy (DMD), homozygous familial hypercholesterolemia (HoFH), acute hepatic porphyria (AHP), and spinal muscular atrophy (SMA) [16, 17]. The diaphragm is less affected than the intercostal muscles. CRISPRCas12a target binding unleashes indiscriminate single-stranded DNase activity. 31, 17171731 (2017). Using Antisense oligonucleotides (ASOs), researchers. The coding region itself appears to be somewhat less targetable. Nat. Genes Dev. 2016;7:11215. Nature 298, 240244 (1982). 2014;56:5566. All experiments were repeated for three times, data were shown as meanSD (A, B, D) or meanSEM (C, E), * P<0.05, ** P<0.01, *** P<0.001, NS P>0.05, in Students test (A, B, D) or paired Students test (C, E). Using Antisense oligonucleotides (ASOs), researchers. K-Selected species, such as pluricellular organisms with specialized tissues and organs, are bigger, have longer life cycles and slow maturation, and their colonization of new environments depends on their ability to adapt physiologically. 5, 2323 (2020). Rev. [121], No compounds have been taken forward to the clinical stage. Efficient base editing with high precision in rabbits using YFE-BE4max. & Laurent, B. Genome Res. J. Pers. Getts, D. R., Shea, L. D., Miller, S. D. & King, N. J. C. Harnessing nanoparticles for immune modulation. Diabetic retinopathy:Antisense oligonucleotides (e.g., iCo-007) are currently under trials for the treatment of diabetic retinopathy. Simhadri, V. L. et al. 3F). Walton, R. T., Christie, K. A., Whittaker, M. N. & Kleinstiver, B. P. Unconstrained genome targeting with near-PAMless engineered CRISPRCas9 variants. is partially funded by NIH grant R21 GM135736. (F) HE staining in liver metastatic foci. r-Selected species, such as bacteria, are small organisms with short life cycles and fast maturation that are able to rapidly populate new environments. PubMed Theranostics. Scoles wrote the manuscript and produced the figures. Alternative splicing of G9a regulates neuronal differentiation. 129, 461467 (2016). ASO Antisense oligonucleotides6kDa Exondys 51 (eteplirsen)DMDexon51(pre-mature termination)EteplirsenmRNAspliceexon51 As a Rho GTPase-family ATPase, the host gene RHOBTB3 is involved in membrane transport [8, 9] and proteasomal degradation [10] and can inhibit tumor growth by promoting the proteasomal degradation of HIF- in renal cancer [11]. Chem. Opin. Small pieces of DNA or RNA that bind to specific molecules of RNA. Sci. The right column diagram shows the quantification analysis results. Modified mRNA directs the fate of heart progenitor cells and induces vascular regeneration after myocardial infarction. Many commercial vectors, such as Lipofectin and compounds known collectively as Eufectins, Cytofectin, Lipofectamine, etc., are commonly used in laboratory research studies. Curr. 36, 888896 (2018). Antisense oligonucleotides (ASOs) are used to selectively inhibit the translation of disease-associated genes via Ribonuclease H (RNaseH)-mediated cleavage or steric hindrance. Another powerful method is to perform transcriptome analysis (RNA-seq) using tissues from mice that are null for the mRNA target, following a treatment trial with the ASO candidate, where differentially expressed genes would indicate off-targets or perhaps incidental cytotoxicity. Risdiplam (marketed as Evrysdi) is a medication taken by mouth in liquid form. Science 345, 11841188 (2014). Med. Leading the way currently in medical use is the ASO drug nusinersen that is approved for treating multiple forms of spinal muscular atrophy (SMA).1 Other ASO therapeutics that are Food and Drug Administration (FDA) approved include eteplirsen for Duchene muscular dystrophy (DMD)2 and inotersen for familial amyloid polyneuropathy (FAP).3. [2][8], The age of onset and the severity of symptoms form the basis of the traditional classification of spinal muscular atrophy into a number of types. Together with previous data, we proposed a novel circRNA exosome secretion mechanism: circRHOBTB3 is specifically sorted into exosomes via the interaction between the ESCRT-II complex member SNF8 and its own specific element and is secreted outside of tumor cells. 9, 2717 (2018). However, the tumor exosomal escape mechanism should still be extensively investigated in the context of other tumor inhibitory molecules, such as miRNAs and proteins. 42, 407408 (2017). Sendai virus, an RNA virus with no risk of genomic integration, delivers CRISPR/Cas9 for efficient gene editing. (J) Relative circRHOBTB3 or RHOBTB3 expression and (K) cell proliferation and (L, M) quantification of cell migration and invasion assay of ASO-NC, ASO-exo, ASO-cir and ASO-cir combined with ASO-exo treated SW480 (L) Mock and (M) KO cells. These data demonstrated that both ASO-cir and ASO-exo might play an antitumor role by specifically targeting circRHOBTB3. Opin. & Blencowe, B. J. Several of these peptides, such as the Drosophila melanogaster homeotic transcription factor, the Antennapedia peptide (96), and the Tat protein of HIV-1 (97), have been identified and studied. Rev. 38, 875882 (2020). Fu, X.-D. & Ares, M. Context-dependent control of alternative splicing by RNA-binding proteins. The overall prevalence of SMA, of all types and across all ethnic groups, is in the range of 1 per 10,000 individuals; the gene frequency is around 1:100, therefore, approximately one in 50 persons are carriers. Because the particle diameter of exosomes is 30nm100nm, which is equivalent to the pore diameter of the glomerular filtration membrane whose filtration limit is 100nm [45], exosomes carrying circRHOBTB3 could be filtered from blood to urine by the glomerulus. Gabut, M. et al. Spiller, D. G., Giles, R. V., Grzybowski, J., Tidd, D. M., and Clark, R. E. Improving the intracellular delivery and molecular efficacy of antisense oligonucleotides in chronic myeloid leukemia cells: a comparison of streptolysin-. Nanoparticle delivery of CRISPR into the brain rescues a mouse model of Fragile X syndrome from exaggerated repetitive behaviours. Immunoblotting assays showed that the epithelial marker E-cadherin was downregulated, but the mesenchymal marker vimentin was upregulated in circRHOBTB3-KO cells (Fig. Moreover, these ASOs could significantly elevate circRHOBTB3 expression in spleen primary foci (Fig. & Davies, K. E. Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment. [72][73][74][75], Children with SMA do not differ from the general population in their behaviour; their cognitive development can be slightly faster, and certain aspects of their intelligence are above the average. Commun. Evolved Cas9 variants with broad PAM compatibility and high DNA specificity. Recently, survival has increased in severe SMA patients with aggressive and proactive supportive respiratory and nutritional support. Biotechnol. To overcome this problem, Partridge et al. ASOs have become a potential therapeutic strategy for diverse malignant diseases along with chemical modification and delivery vehicle development. Following R-loop formation, the unpaired or single-stranded DNA is accessible for base editing. Cell 73, 10661074 (2019). Goodman, K. M. et al. Nat Cell Biol. Weng W, Wei Q, Toden S, Yoshida K, Nagasaka T, Fujiwara T, et al. The authors declare no competing interests. Moreover, the overexpression of circRHOBTB3 did not change the expression of the host gene RHOBTB3 (Fig. 2019;1871:45568. Bergan, R., Connell, Y., Fahmy, B., and Neckers, L. Electroporation enhances c-. Cell Res. Data were shown as meanSD (A, B, C, D, E, H, I, L, M, N, O, Q, X) or meanSEM (F, J), * P<0.05, ** P<0.01, *** P<0.001, NS P>0.05, in Students test (A, B, C, D, E, H, I, L, M, N, O, Q, R) or paired Students test (F, J). Lee Y, Rio DC. 2D and S3A), which showed that circRHOBTB3 could inhibit cell proliferation (Fig. 2P). The .gov means its official. PubMedGoogle Scholar. Base editing: advances and therapeutic opportunities. Engineered CRISPRCas12a variants with increased activities and improved targeting ranges for gene, epigenetic and base editing. Skorski, T., Perrotti, D., Nieborowska-Skorska, M., Gryaznov, S., and Calabretta, B. Antileukemia effect of c-. (A) Observation of CRC cell exosomes by transmission electron microscopy (TEM) and Western blotting with anti-CD63 and anti-TSG101 antibodies. Tumor initiation and progression remain poorly understood despite the evidence that this kind of somatic evolutionary process was driven by the accumulation of genetic alterations [30]. Irimia, M. & Blencowe, B. J. about navigating our updated article layout. Bak, R. O. Cell 123, 6573 (2005). Histone marks regulate the epithelial-to-mesenchymal transition via alternative splicing. D.R. Nat Genet. Intriguingly, we found that circRHOBTB3 was abundantly enriched in urine. Tress, M. L., Abascal, F. & Valencia, A. [60][61] Risdiplam was first approved for medical use in the United States in August 2020[58] and has since been approved in over 30 countries. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. All experiments were repeated for three times, data were shown as meanSD (B, C, D, F, G,J, K) or meanSEM (E, H, I, L, M), * P<0.05, ** P<0.01, *** P<0.001, NS P>0.05, in Students test (B, C, D, F, G,J, K) or paired Students test (E, H, I, L, M). (2020) and Zhang et al. Engineering of CRISPRCas12b for human genome editing. 379, 6473 (2018). [9][1], Usually, the mutation in the SMN1 gene is inherited from both parents in an autosomal recessive manner, although in around 2% of cases it occurs during early development (de novo). Sci. This denotes the adult-onset form, sometimes also classified as a late-onset SMA type 3. Schor, I. E., Rascovan, N., Pelisch, F., All, M. & Kornblihtt, A. R. Neuronal cell depolarization induces intragenic chromatin modifications affecting NCAM alternative splicing. When sterically blocking oligonucleotides are used, Northern blotting becomes irrelevant as these oligonucleotides do not induce mRNA cleavage by the RNase H. To demonstrate antisense efficacy, one can, e.g., demonstrate the synthesis of a truncated peptide (34). The top lead ASO was designated ASO7 and lowered ATXN2 expression in SCA2 mouse cerebella by >60% for up to 13 weeks, without activating markers of gliosis. Nat Rev Mol Cell Biol. Ma, Y. et al. Sci. S8C). One useful approach is to perform quantitative PCR to assess expression of mRNAs with target sequences including mismatches to the ASO candidate to ensure unchanged expression. De novo design of bioactive protein switches. 67, 6776 (2021). (C) Expression of circRHOBTB3 in ASO-NC- and ASO-cir-treated HCT116 cells. Rev. ASO inhibits CRC cell growth and metastasis in vivo. All experiments were repeated for three times, data were shown as meanSD (B) or meanSEM (D), * P<0.05, ** P<0.01, *** P<0.001, NS P>0.05, in Students test (B) or paired Students test (D). 2016;26:127787. RHOBTB3 promotes proteasomal degradation of HIF through facilitating hydroxylation and suppresses the Warburg effect. This bond effectively locks the base into a conformation predominantly characterizing the RNA ribose sugar and prevents the conformation characteristic of the deoxyribose sugar.14 The benefit of locked nucleic acids (LNAs) is that they can produce both increased target specificity and reduced recognition by nucleases. Cell 176, 254267 (2019). https://doi.org/10.1186/s12943-022-01511-1, DOI: https://doi.org/10.1186/s12943-022-01511-1. This partly depends on the number of copies of the SMN2 gene present on the chromosome. (D) Western blotting of SNF8-KD HCT116 cells transfected with siRNA using anti-SNF8. CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations. Hum. and JavaScript. Penev, A. et al. Difficulty achieving developmental milestones, difficulty sitting/standing/walking, In small children: adopting of a frog-leg position when sitting (hips abducted and knees flexed), Bell-shaped torso (caused by using only abdominal muscles for respiration) in severe SMA type, Reldesemtiv (CK-2127107, CK-107) is a skeletal. Mol. Curr. Mol Ther Nucleic Acids. S8E). Givens, B. E., Naguib, Y. W., Geary, S. M., Devor, E. J. 27, 154157 (2017). Biol. Nat. Mol. A recently developed genome editing technology that, like base editing, does not rely on double-stranded breaks. SMA type 3 can have similar respiratory problems, but it is more rare. Enhanced base editing by co-expression of free uracil DNA glycosylase inhibitor. Biotechnol. These second-generation oligonucleotides are resistant to degradation by cellular nucleases and hybridize specifically to their target mRNA with higher affinity than the isosequential phosphodiester or phosphorothioate. Body muscles are weakened, and the respiratory system is a major concern as are muscle contractures and spinal curvature. Yin, H. et al. Get time limited or full article access on ReadCube. 36, 395402 (2015). Biol. Determinants of base editing outcomes from target library analysis and machine learning. J. Mol. Consequently, denervated muscles undergo progressive atrophy (waste away). Nat. FOIA The possible mechanism is that this cis-element acts as an ESS bound to some RBPs to impede spliceosome activity and block circRHOBTB3 circularization. 9, 1621 (2021). Per the name, FSHD tends to sequentially weaken the muscles of the face, those that position the scapula, and those overlying the humerus bone of the upper arm. Proc. PubMed 2009;296:F94756. Vasc. Sasaguri, H. et al. (G) Expression of circRHOBTB3 in xenograft tumors, (G) plasma, and (I) urine with tail vein injection of ASO-combined or ASO-NC. Tanaka, S. et al. Bladen, C. L. et al. Nat. The resulting RNA-mRNA duplex is then believed to be cleaved to a series of 2123-mers by the RNA III-related enzyme Dicer (7375). & Porteus, M. H. CRISPR-mediated integration of large gene cassettes using AAV donor vectors. et al. 26, 524541 (2018). A., Metkar, M. & Moore, M. J. 45, 498506 (1989). Article (Q) Expression of circRHOBTB3 in the plasma and (R) urine of mice inoculated with control or circRHOBTB3-OE HCT116 cells.
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