Association between abnormal expression and methylation of LGALS1 in amyotrophic lateral sclerosis

被引:6
作者
Cai, Zhengyi [1 ]
Yin, Kaili [2 ]
Liu, Qing [1 ]
Liu, Mingsheng [1 ]
Yang, Xunzhe [1 ]
Cui, Liying [1 ,3 ,4 ]
机构
[1] Peking Union Med Coll & Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Neurol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll, McKusick Zhang Ctr Genet Med, State Key Lab Med Mol Biol,Inst Basic Med Sci,Sch, Beijing, Peoples R China
[3] Chinese Acad Med Sci, Neurosci Ctr, Beijing, Peoples R China
[4] Peking Union Med Coll & Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Neurol, Beijing 100730, Peoples R China
关键词
Amyotrophic lateral sclerosis; LGALS1; Galectin-1; DNA methylation; DNA METHYLATION; GALECTIN-1; ALS;
D O I
10.1016/j.brainres.2022.148022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: DNA methylation has been identified to play an important role in amyotrophic lateral sclerosis (ALS). Galectin-1, encoded by LGALS1 gene, has been proved to be associated with ALS. We aimed to investigate the association between the expression and methylation of LGALS1 in blood samples from ALS patients.Methods: Forty-five patients diagnosed with ALS were enrolled. Thirty-two healthy relatives consisted the control group. Among them, samples from 12 patients and 12 controls consisted the exploration samples. In the exploration samples, mRNA expression levels were detected by quantitative real-time PCR. In all the samples, DNA methylation levels of one CpG island containing 12 CpG sites in the gene promoter were detected by bisulfite sequencing PCR, and galectin-1 levels were examined by enzyme linked immunosorbent assay. Asso-ciations between the gene expression and methylation level, as well as between the region-specific methylation level and clinical variables were calculated. Results: The mRNA expression level of LGALS1 was significantly increased and the promoter of LGALS1 was hypomethylated in ALS patients. Serum galectin-1 levels were significantly elevated in the ALS patients. The ALS group had significantly lower methylation level at certain CpG sites than the control group. There were signif-icant negative associations between abnormal expression and methylation of LGALS1, as well as between region -specific methylation levels and the age of onset.Conclusions: The aberrant expression and DNA methylation of LGALS1 and their association reveals epigenetic changes in ALS patients, which are helpful for early intervention and treatment for the disease.
引用
收藏
页数:8
相关论文
共 25 条
[1]   Inflammatory Gene Expression in Whole Peripheral Blood at Early Stage of Sporadic Amyotrophic Lateral Sclerosis [J].
Andres-Benito, Pol ;
Moreno, Jesus ;
Dominguez, Raul ;
Aso, Ester ;
Povedano, Monica ;
Ferrer, Isidro .
FRONTIERS IN NEUROLOGY, 2017, 8
[2]   El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis [J].
Brooks, BR ;
Miller, RG ;
Swash, M ;
Munsat, TL .
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05) :293-299
[3]  
Brown RH, 2017, NEW ENGL J MED, V377, P162, DOI [10.1056/NEJMc1710379, 10.1038/nrdp.2017.85, 10.1056/NEJMra1603471, 10.1016/S0140-6736(10)61156-7, 10.1016/S0140-6736(17)31287-4]
[4]   Neuroprotective effect of oxidized galectin-1 in a transgenic mouse model of amyotrophic lateral sclerosis [J].
Chang-Hong, R ;
Wada, M ;
Koyama, S ;
Kimura, H ;
Arawaka, S ;
Kawanami, T ;
Kurita, K ;
Kadoya, T ;
Aoki, M ;
Itoyama, Y ;
Kato, T .
EXPERIMENTAL NEUROLOGY, 2005, 194 (01) :203-211
[5]   Gene profiling of skeletal muscle in an amyotrophic lateral sclerosis mouse model [J].
de Aguilar, Jose-Luis Gonzalez ;
Niederhauser-Wiederkehr, Christa ;
Halter, Benoit ;
De Tapia, Marc ;
Di Scala, Franck ;
Demougin, Philippe ;
Dupuis, Luc ;
Primig, Michael ;
Meininger, Vincent ;
Loeffler, Jean-Philippe .
PHYSIOLOGICAL GENOMICS, 2008, 32 (02) :207-218
[6]   Epigenetic mechanisms in amyotrophic lateral sclerosis: A short review [J].
Dolinar, Ana ;
Ravnik-Glavac, Metka ;
Glavac, Damjan .
MECHANISMS OF AGEING AND DEVELOPMENT, 2018, 174 :103-110
[7]   Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease [J].
Ebbert, Mark T. W. ;
Ross, Christian A. ;
Pregent, Luc J. ;
Lank, Rebecca J. ;
Zhang, Cheng ;
Katzman, Rebecca B. ;
Jansen-West, Karen ;
Song, Yuping ;
da Rocha, Edroaldo Lummertz ;
Palmucci, Carla ;
Desaro, Pamela ;
Robertson, Amelia E. ;
Caputo, Ana M. ;
Dickson, Dennis W. ;
Boylan, Kevin B. ;
Rademakers, Rosa ;
Ordog, Tamas ;
Li, Hu ;
Belzil, Veronique V. .
ACTA NEUROPATHOLOGICA, 2017, 134 (05) :715-728
[8]   Identification of Epigenetically Altered Genes in Sporadic Amyotrophic Lateral Sclerosis [J].
Figueroa-Romero, Claudia ;
Hur, Junguk ;
Bender, Diane E. ;
Delaney, Colin E. ;
Cataldo, Michael D. ;
Smith, Andrea L. ;
Yung, Raymond ;
Ruden, Douglas M. ;
Callaghan, Brian C. ;
Feldman, Eva L. .
PLOS ONE, 2012, 7 (12)
[9]   Expression and functions of galectin-1 in sensory and motoneurons [J].
Gaudet, AD ;
Steeves, JD ;
Tetzlaff, W ;
Ramer, MS .
CURRENT DRUG TARGETS, 2005, 6 (04) :419-425
[10]   Galectin-1 is a component of neurofilamentous lesions in sporadic and familial amyotrophic lateral sclerosis [J].
Kato, T ;
Kurita, K ;
Seino, T ;
Kadoya, T ;
Horie, H ;
Wada, M ;
Kawanami, T ;
Daimon, M ;
Hirano, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 282 (01) :166-172