Evidence map›Paper›PMID 39533002›Full record

ArticleScientific reports2024

Stabilization of a single-stranded DNA of adeno-associated virus by inverted terminal repeats.

Yuzhe Yuan, Kiyoko Higashiyama, Emi Ito-Kudo, Kyoko Masumi-Koizumi, Keisuke Yusa, Kazuhisa Uchida

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Yuzhe YuanGraduate School of Science, Technology, and Innovation, Kobe University, 7-1-49 Minatojima Minamimachi, Chuo-ku, Kobe, 650-0047, Japan.
Kiyoko HigashiyamaGraduate School of Science, Technology, and Innovation, Kobe University, 7-1-49 Minatojima Minamimachi, Chuo-ku, Kobe, 650-0047, Japan.
Emi Ito-KudoGraduate School of Science, Technology, and Innovation, Kobe University, 7-1-49 Minatojima Minamimachi, Chuo-ku, Kobe, 650-0047, Japan.
Kyoko Masumi-KoizumiGraduate School of Science, Technology, and Innovation, Kobe University, 7-1-49 Minatojima Minamimachi, Chuo-ku, Kobe, 650-0047, Japan.
Keisuke YusaGraduate School of Science, Technology, and Innovation, Kobe University, 7-1-49 Minatojima Minamimachi, Chuo-ku, Kobe, 650-0047, Japan.
Kazuhisa UchidaGraduate School of Science, Technology, and Innovation, Kobe University, 7-1-49 Minatojima Minamimachi, Chuo-ku, Kobe, 650-0047, Japan. kazuhisa.uchida@port.kobe-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parvoviruses have evolved to possess a linear single-stranded DNA (ssDNA) genome ranging from 4 to 6.3 kb. Adeno-associated virus (AAV), a member of the Parvoviridae family, contains approximately 5 kb of linear ssDNA within its capsid. This ssDNA features two 145-base inverted terminal repeats (ITRs) positioned at each end. ITRs have a T-shaped hairpin secondary structure, which plays a crucial role in viral replication. To investigate the impact of ITRs on ssDNA stability, we conducted a DNA denaturation-reannealing assay in 10 mM magnesium acetate, 50 mM potassium acetate, and 20 mM Tris-acetate buffer at pH7.9. Conventional double-stranded DNA (dsDNA) fragments retain a reannealing capability of over 50% for sizes under 8.8 kb, gradually losing this capability as sizes increase; however, dsDNA fragments in rAAV ranging from 0.7 to 6.3 kb did not exhibit a reannealing profile. This suggests that the presence of ITRs at both ends hinders annealing between the complementary strands. These results indicate that ITR structures preferentially induce an ssDNA conformation less than 6.3 kb in size, and that the stability of AAV ssDNA contributes to the viral life cycle, including processes such as infection, replication, and packaging. Considering the size of parvovirus genomes, it appears that their genomes require reversible flexibility in complementary DNA strands; simultaneously, this adaptability needs to be regulated by specific palindromic ITRs at both ends.

Indexed as

DependovirusDNA, Single-StrandedDNA, ViralTerminal Repeat SequencesGenome, ViralHumansNucleic Acid ConformationNucleic Acid DenaturationDNA, Single-StrandedDNA, ViralAdeno-associated virusInverted terminal repeatParvovirusSingle-stranded DNA

Identifiers

PMID39533002
PMCPMC11557940

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.