Global Repeat Map (GRM): Advantageous Method for Discovery of Largest Higher-Order Repeats (HORs) in Neuroblastoma Breakpoint Family (NBPF) Genes, in Hornerin Exon and in Chromosome 21 Centromere.

Q2 Medicine
Vladimir Paar, Ines Vlahović, Marija Rosandić, Matko Glunčić
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引用次数: 0

Abstract

Here we present three interesting novel human Higher-Order Repeats (HORs) discovered using the HOR-searching method with GRM algorithm: (a) The novel Neuroblastoma Breakpoint Family gene (NBPF) 3mer HOR, discovered applying GRM algorithm to human chromosome 1 (Paar et al., Mol Biol Evol 28:1877-1892, 2011). NBPF 3mer HOR is based on previously known ~1.6 kb NBPF primary repeat monomers (known as DUF1220 domain) in human chromosome 1, but the NBPF HOR was not known before its discovery by using GRM. It should be stressed that the NBPF HOR presents a unique human-specific pattern, distinguishing human from nonhuman primates. (b) The novel quartic HOR (2mer⊃2mer⊃9mer) discovered using the GRM algorithm for analysis of hornerin genes in human chromosome 1 (Paar et al., Mol Biol Evol 28:1877-1892, 2011). This quartic HOR is based on 39 bp hornerin primary repeat monomer in human chromosome 1. To our knowledge, this is the first known case of quartic HOR, with four levels of hierarchy of HOR organization. (c) The novel 33mer alpha satellite HOR in human chromosome 21, discovered using the GRM algorithm (Glunčić et al., Sci Rep 9:12629, 2019). This 33mer HOR in the smallest human chromosome is the largest alpha satellite HOR copy among all 22 somatic human chromosomes. Moreover, the same 33mer HOR is present in the hg38 human genome assembly of four human chromosomes: 21, 22, 13, and 14. We point out that the DUF1220 encoding genomic structures in NBPF genes in human chromosome 1, recently studied and related to the brain evolution and pathologies and cognitive aptitude, can be considered in the framework of the general concept of HORs, already extensively studied in genomics, especially in the centromeric region.

全球重复序列图谱(GRM):发现神经母细胞瘤断点家族(NBPF)基因、角蛋白外显子和21号染色体着丝粒中最大高阶重复序列(HORs)的有利方法。
在此,我们介绍了使用GRM算法的高阶重复序列搜索方法发现的三个有趣的新的人类高阶重复序列(HORs): (a)利用GRM算法在人类1号染色体上发现的新的神经母细胞瘤断点家族基因(NBPF) 3mer HOR (Paar等人,Mol Biol evolution 28:1877-1892, 2011)。NBPF 3mer HOR是基于人类1号染色体中已知的约1.6 kb的NBPF一级重复单体(称为DUF1220结构域),但NBPF的HOR在使用GRM发现之前并不为人所知。应该强调的是,NBPF HOR呈现出一种独特的人类特异性模式,将人类与非人灵长类动物区分开来。(b)使用GRM算法发现了新的四次HOR (2mer、2mer、9mer),用于分析人类1号染色体上的激素基因(Paar等人,Mol Biol Evol 28:1877-1892, 2011)。该四分位HOR基于人类1号染色体上39 bp的角蛋白初级重复单体。据我们所知,这是第一个已知的四次HOR病例,具有四个层次的HOR组织。(c)利用GRM算法在人类21号染色体上发现的新33mer α卫星HOR (glun等人,科学进展9:12629,2019)。这个最小的人类染色体上的33mer HOR是所有22条体细胞人类染色体中最大的α卫星HOR拷贝。此外,同样的33聚体HOR存在于人类基因组的4条染色体:21、22、13和14的hg38中。我们指出,编码人类1号染色体NBPF基因基因组结构的DUF1220最近被研究并与大脑进化、病理和认知能力有关,可以在HORs的一般概念框架中考虑,HORs已经在基因组学中广泛研究,特别是在着丝粒区域。
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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
7
期刊介绍: Molecular biology has been providing an overwhelming amount of data on the structural components and molecular machineries of the cell and its organelles and the complexity of intra- and intercellular communication. The molecular basis of hereditary and acquired diseases is beginning to be unravelled, and profound new insights into development and evolutionary biology have been gained from molecular approaches. Progress in Molecular and Subcellular Biology summarises the most recent developments in this fascinating area of biology.
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