Mohammad Rabiul Karim, Ahmed I Abo-Ahmed, Abu Raihan, Md Asif Karim Hemel, Md Alamgir Kobir, Munmun Pervin
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The ABI Prism 3100 Genetic Analyzer was used to analyze the sequences of the corresponding cDNA fragments.</p><p><strong>Results: </strong>In RT-PCR, the findings unequivocally demonstrated that the pigeon brain's cerebellum, optic tectum, thalamus, and telencephalon all expressed the mRNA for GluN2B. The cDNA sequence of pigeon GluN2B was obtained from PCR-amplified products and included 51 base pairs (bp) of the 5' untranslated region (UTR), a 4,512-bp open reading frame, and 13 bps of the 3' UTR. Pigeon GluN2B's cDNA sequencing displayed 85% identity for human GluN2B and 95% identity for chicken. The amino acid sequences encoded by the pigeon GluN2B gene shared between 85% and 97% similarity with those of humans, rats, and mice. Molecular phylogenetic analysis using the neighbor-joining method showed that pigeon GluN2B is closely related to the GluN2B proteins of these other species.</p><p><strong>Conclusion: </strong>The findings suggest that certain neurons in the pigeon brain GluN2B mRNA. They also indicate the presence of various glutamatergic networks and connections within the avian brain.</p>","PeriodicalId":14892,"journal":{"name":"Journal of Advanced Veterinary and Animal Research","volume":"12 2","pages":"427-432"},"PeriodicalIF":1.5000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12506696/pdf/","citationCount":"0","resultStr":"{\"title\":\"GluN2B mRNA expression and molecular sequence in the brain of pigeons (<i>Columba livia</i>).\",\"authors\":\"Mohammad Rabiul Karim, Ahmed I Abo-Ahmed, Abu Raihan, Md Asif Karim Hemel, Md Alamgir Kobir, Munmun Pervin\",\"doi\":\"10.5455/javar.2025.l909\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>The current study sought to ascertain the mRNA expression and establish the complementary DNA (cDNA) sequences of pigeon brain's glutamate receptor 2B of N-methyl-D-aspartate (GluN2B) type.</p><p><strong>Material and methods: </strong>Adult pigeons (<i>Columba livia; n</i> = 8, sharing an equal number of males and females) were used. After proper anesthesia, the brain was exposed, and small pieces of cerebellum, optic tectum, thalamus, and telencephalon were collected quickly; total ribonucleic acid (RNA) was isolated, and cDNA was synthesized for PCR amplification. The ABI Prism 3100 Genetic Analyzer was used to analyze the sequences of the corresponding cDNA fragments.</p><p><strong>Results: </strong>In RT-PCR, the findings unequivocally demonstrated that the pigeon brain's cerebellum, optic tectum, thalamus, and telencephalon all expressed the mRNA for GluN2B. The cDNA sequence of pigeon GluN2B was obtained from PCR-amplified products and included 51 base pairs (bp) of the 5' untranslated region (UTR), a 4,512-bp open reading frame, and 13 bps of the 3' UTR. Pigeon GluN2B's cDNA sequencing displayed 85% identity for human GluN2B and 95% identity for chicken. The amino acid sequences encoded by the pigeon GluN2B gene shared between 85% and 97% similarity with those of humans, rats, and mice. Molecular phylogenetic analysis using the neighbor-joining method showed that pigeon GluN2B is closely related to the GluN2B proteins of these other species.</p><p><strong>Conclusion: </strong>The findings suggest that certain neurons in the pigeon brain GluN2B mRNA. 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引用次数: 0
摘要
目的:研究鸽脑n -甲基- d -天冬氨酸(GluN2B)型谷氨酸受体2B的mRNA表达,建立互补DNA (cDNA)序列。材料和方法:选用成年鸽子(Columba livia, n = 8,雌雄相等)。适当麻醉后,暴露大脑,迅速收集小脑、视顶叶、丘脑和端脑的小块;分离总核糖核酸(RNA),合成cDNA进行PCR扩增。使用ABI Prism 3100基因分析仪分析相应cDNA片段的序列。结果:RT-PCR结果明确表明,鸽子大脑小脑、视顶叶、丘脑和端脑均表达GluN2B mRNA。从pcr扩增产物中获得鸽GluN2B的cDNA序列,包括51个碱基对(bp)的5‘非翻译区(UTR),一个4512bp的开放阅读框和13个bps的3’ UTR。鸽子GluN2B基因序列与人GluN2B的同源性为85%,与鸡GluN2B基因的同源性为95%。鸽子GluN2B基因编码的氨基酸序列与人类、大鼠和小鼠的氨基酸序列有85%到97%的相似性。分子系统发育分析表明,鸽子GluN2B蛋白与其他物种的GluN2B蛋白具有密切的亲缘关系。结论:研究结果提示,鸽子脑内的某些神经元GluN2B mRNA表达。它们还表明鸟类大脑中存在各种谷氨酸能网络和连接。
GluN2B mRNA expression and molecular sequence in the brain of pigeons (Columba livia).
Objectives: The current study sought to ascertain the mRNA expression and establish the complementary DNA (cDNA) sequences of pigeon brain's glutamate receptor 2B of N-methyl-D-aspartate (GluN2B) type.
Material and methods: Adult pigeons (Columba livia; n = 8, sharing an equal number of males and females) were used. After proper anesthesia, the brain was exposed, and small pieces of cerebellum, optic tectum, thalamus, and telencephalon were collected quickly; total ribonucleic acid (RNA) was isolated, and cDNA was synthesized for PCR amplification. The ABI Prism 3100 Genetic Analyzer was used to analyze the sequences of the corresponding cDNA fragments.
Results: In RT-PCR, the findings unequivocally demonstrated that the pigeon brain's cerebellum, optic tectum, thalamus, and telencephalon all expressed the mRNA for GluN2B. The cDNA sequence of pigeon GluN2B was obtained from PCR-amplified products and included 51 base pairs (bp) of the 5' untranslated region (UTR), a 4,512-bp open reading frame, and 13 bps of the 3' UTR. Pigeon GluN2B's cDNA sequencing displayed 85% identity for human GluN2B and 95% identity for chicken. The amino acid sequences encoded by the pigeon GluN2B gene shared between 85% and 97% similarity with those of humans, rats, and mice. Molecular phylogenetic analysis using the neighbor-joining method showed that pigeon GluN2B is closely related to the GluN2B proteins of these other species.
Conclusion: The findings suggest that certain neurons in the pigeon brain GluN2B mRNA. They also indicate the presence of various glutamatergic networks and connections within the avian brain.