Literature DB >> 32304783

Allele frequency analysis of GALC gene causing Krabbe disease in human and its codon usage.

Debaroti Das1, Bornali Deb1, Arup Kumar Malakar1, Supriyo Chakraborty2.   

Abstract

Krabbe disease is one of the rarest autosomal recessive disorders in human, caused by mutation in the GALC (β-galactosylceramidase) gene, resulting in several mental and physical health issues. Due to its rarity and phenotypic heterogeneity, diagnosis rate of this disease is very low. This study generated information on the recessive allele frequency dynamics of GALC gene across 15 global populations, with the highest frequency detected in Druze (Israel) population and the lowest frequency in Turkey and the United States. The recessive allele would take more time period (about 24,975 years) to be completely removed from the population having the lowest frequency and vice versa. The codon usage patterns of four isoforms of GALC gene revealed that a few synonymous codons were used more frequently than others in the isoforms. The codon AGA (arginine) was found to be overrepresented in GALC gene, except for galactocerebrosidase isoform a precursor. Further, GALC gene showed low codon usage bias (CUB) as evident from high ENC values (55.7-58.2), with A/T ending codons more preferred to G/C ending codons. CUB analysis elucidated the dual role of mutational pressure (major role) and natural selection (minor role) in GALC gene evolution.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  GALC gene; Galactocerebrosidase isoform a, c, d, X1; Krabbe disease

Year:  2020        PMID: 32304783     DOI: 10.1016/j.gene.2020.144673

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  2 in total

1.  Two Cases of Female Chinese Adult-Onset Krabbe Disease with One Novel Mutation and a Review of Literature.

Authors:  Chengyi Zhang; Zheng Liu; Huiqing Dong
Journal:  J Mol Neurosci       Date:  2020-11-14       Impact factor: 3.444

2.  Calculating and comparing codon usage values in rare disease genes highlights codon clustering with disease-and tissue- specific hierarchy.

Authors:  Rachele Rossi; Mingyan Fang; Lin Zhu; Chongyi Jiang; Cong Yu; Cristina Flesia; Chao Nie; Wenyan Li; Alessandra Ferlini
Journal:  PLoS One       Date:  2022-03-31       Impact factor: 3.240

  2 in total

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