2013
DOI: 10.1039/c3mb25391k
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Genomics and proteomics in solving brain complexity

Abstract: The human brain is extraordinarily complex, composed of billions of neurons and trillions of synaptic connections. Neurons are organized into circuit assemblies that are modulated by specific interneurons and non-neuronal cells, such as glia and astrocytes. Data on human genome sequences predicts that each of these cells in the human brain has the potential of expressing ∼20 000 protein coding genes and tens of thousands of noncoding RNAs. A major challenge in neuroscience is to determine (1) how individual ne… Show more

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Cited by 21 publications
(12 citation statements)
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References 185 publications
(223 reference statements)
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“…Identifying the composition and dynamics of the synaptic proteome is key to understanding the remodeling of existing synapses and growth of new synapses, as well as identifying novel therapeutic targets for synaptopathies (7,8). The composition of the synaptic proteome is determined by proteins transported from the cell body and local synthesis of proteins at the synapses.…”
mentioning
confidence: 99%
“…Identifying the composition and dynamics of the synaptic proteome is key to understanding the remodeling of existing synapses and growth of new synapses, as well as identifying novel therapeutic targets for synaptopathies (7,8). The composition of the synaptic proteome is determined by proteins transported from the cell body and local synthesis of proteins at the synapses.…”
mentioning
confidence: 99%
“…Genomics is rapidly being used to understand the structure and function of all the genes and other biological features in the entire DNA sequence of the organism along with comparison of genome. It is a discipline that applies DNA sequencing methods, recombinant DNA and bioinformatics to sequence, assemble and analyse the structure and function of genomes (that is a complete set of DNA within a single cell of an organism) [18,19]. A great revolution has been elicited with the advancement in genomic studies to uncover the complexity of human genome and make easy to understand about the difficulty of biological system [20].…”
Section: Genomic Approachesmentioning
confidence: 99%
“…Sequencing can be done either unidirectional (single-end sequencing) or bidirectional (paired-end sequencing) and then aligned to a reference genome database or assembled to obtain de novo transcripts, proving a genome-wide expression profile (Wang et al, 2009). The advantages of RNA-Seq and its application in studying nervous system and the challenges associated with the technology are summarized in a previous publication (Kadakkuzha and Puthanveettil, 2013). Unlike microarray technology, which depends on already known genes, RNA-Seq is not dependent on existing genome data and can screen novel transcript and analyze transcript structure, including single base-pair resolution and exonic boundaries, which is very valuable while investigating SNPs, thus making it useful for genotyping and linkage analysis (Wang et al, 2009).…”
Section: Rna-seqmentioning
confidence: 99%