Evidence map›Paper›PMID 40490738›Full record

ArticleBMC bioinformatics2025

SEQSIM: A novel bioinformatics tool for comparisons of promoter regions-a case study of calcium binding protein spermatid associated 1 (CABS1).

Joy Ramielle L Santos, Weijie Sun, A Dean Befus, Marcelo Marcet-Palacios

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Joy Ramielle L Santos *Department of Medicine, University of Alberta, Edmonton, T6G 2R3, Canada. joyramie@ualberta.ca.
Weijie SunDepartment of Computer Sciences, University of Alberta, Edmonton, T6G 2E1, Canada.
A Dean BefusDepartment of Medicine, University of Alberta, Edmonton, T6G 2R3, Canada.
Marcelo Marcet-Palacios *Department of Medicine, University of Alberta, Edmonton, T6G 2R3, Canada.

Funding

Natural Sciences and Engineering Research Council of Canada RGPIN-2020-04553
6 · The paper itself

Abstract

backgroundUnderstanding transcriptional regulation requires an in-depth analysis of promoter regions, which house vital cis-regulatory elements such as core promoters, enhancers, and silencers. Despite the significance of these regions, genome-wide characterization remains a challenge due to data complexity and computational constraints. Traditional bioinformatics tools like Clustal Omega face limitations in handling extensive datasets, impeding comprehensive analysis. To bridge this gap, we developed SEQSIM, a sequence comparison tool leveraging an optimized Needleman-Wunsch algorithm for high-speed comparisons. SEQSIM can analyze complete human promoter datasets in under an hour, overcoming prior computational barriers.

resultsApplying SEQSIM, we conducted a case study on CABS1, a gene associated with spermatogenesis and stress response but lacking well-defined functions. Our genome-wide promoter analysis revealed 41 distinct homology clusters, with CABS1 residing within a cluster that includes promoters of genes such as VWCE, SPOCK1, and TMX2. These associations suggest potential co-regulatory networks. Additionally, our findings unveiled conserved promoter motifs and long-range regulatory sequences, including LINE-1 transposable element fragments shared by CABS1 and nearby genes, implying evolutionary conservation and regulatory significance.

conclusionsThese results provide insight into potential gene regulation mechanisms, enhancing our understanding of transcriptional control and suggesting new pathways for functional exploration. Future studies incorporating SEQSIM could elucidate co-regulatory networks and chromatin interactions that impact gene expression.

Indexed as

Calcium-Binding ProteinsComputational BiologyPromoter Regions, GeneticSoftwareAlgorithmsHumansMaleCalcium-Binding ProteinsCABS1 gene regulationchromatin architecturePromoter sequence similaritySEQSIM algorithmtransposable elements

Identifiers

PMID40490738
PMCPMC12150522

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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.