Evidence map›Paper›PMID 35655139›Full record

ArticleBMC genomics2022

Frameshift and wild-type proteins are often highly similar because the genetic code and genomes were optimized for frameshift tolerance.

Xiaolong Wang, Quanjiang Dong, Gang Chen, Jianye Zhang, Yongqiang Liu, Yujia Cai

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
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

10 citing papers in PubMed, 20 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Xiaolong WangDepartment of Biotechnology, College of Marine Life Sciences, Ocean University of China, No. 5 Yushan Road, Shandong, Qingdao, 266003, P. R. China. Xiaolong@ouc.edu.cn.
Quanjiang DongQingdao Municipal Hospital, Qingdao, Shandong, 266003, P. R. China.
Gang ChenDepartment of Biotechnology, College of Marine Life Sciences, Ocean University of China, No. 5 Yushan Road, Shandong, Qingdao, 266003, P. R. China.
Jianye ZhangDepartment of Biotechnology, College of Marine Life Sciences, Ocean University of China, No. 5 Yushan Road, Shandong, Qingdao, 266003, P. R. China.
Yongqiang LiuDepartment of Biotechnology, College of Marine Life Sciences, Ocean University of China, No. 5 Yushan Road, Shandong, Qingdao, 266003, P. R. China.
Yujia CaiDepartment of Biotechnology, College of Marine Life Sciences, Ocean University of China, No. 5 Yushan Road, Shandong, Qingdao, 266003, P. R. China.
Ocean University of China · CNQingdao Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Frameshift mutations have been considered of significant importance for the molecular evolution of proteins and their coding genes, while frameshift protein sequences encoded in the alternative reading frames of coding genes have been considered to be meaningless. However, functional frameshifts have been found widely existing. It was puzzling how a frameshift protein kept its structure and functionality while substantial changes occurred in its primary amino-acid sequence. This study shows that the similarities among frameshifts and wild types are higher than random similarities and are determined at different levels. Frameshift substitutions are more conservative than random substitutions in the standard genetic code (SGC). The frameshift substitutions score of SGC ranks in the top 2.0-3.5% of alternative genetic codes, showing that SGC is nearly optimal for frameshift tolerance. In many genes and certain genomes, frameshift-resistant codons and codon pairs appear more frequently than expected, suggesting that frameshift tolerance is achieved through not only the optimality of the genetic code but, more importantly, the further optimization of a specific gene or genome through the usages of codons/codon pairs, which sheds light on the role of frameshift mutations in molecular and genomic evolution.

Indexed as

AlgorithmsFrameshift MutationCodonGenetic CodeProteinsCodonProteins

Identifiers

PMID35655139
PMCPMC9164415
OpenAlexW4281725104

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.