Speaker: HU Xue-Jia Supervisor: WU Yun-Dong Date: 19/12/2013

Introduction – Regulatory codes – “Duons” – Genomic footprint TFs densely populate and evolutionarily constrain protein-coding exons TFs modulate global codon biases Genetic variation in duons frequently alters TF occupancy Summary and perspective 2

Introduction – Regulatory codes – “Duons” – Genomic footprint TFs densely populate and evolutionarily constrain protein-coding exons TFs modulate global codon biases Genetic variation in duons frequently alters TF occupancy Summary and perspective 3

4 Despite redundancy in the genetic code, the choice of codons used is highly biased in some proteins, suggesting that additional constraints operate in certain protein-coding regions of the genome. There are many kinds of regulatory elements within protein coding regions (such as transcription factor binding) those can influence codon choice and amino acid preference that are independent of protein structure or function. Weatheritt, R J.; Badu, M M. Sceicne. 2013, 342:

5 The genetic and regulatory codes have been assumed to operate independently of one another and to be segregated physically into the coding and noncoding genomic compartments. The potential for some coding exons to accommodate transcriptional enhancers or splicing signals has long been recognized. “Duons”: dual-use codons (simultaneously specify both amino acids and TF recognition sites) TF: transcription factor Stergachis, A J.; et al. Sceicne. 2013, 342:

6 A method of investigating the sequence specificity of DNA- binding proteins in vitro. This technique can be used to study protein-DNA interactions both outside and within cells.

Introduction – Regulatory codes – “Duons” – Genomic footprint TFs densely populate and evolutionarily constrain protein-coding exons TFs modulate global codon biases Genetic variation in duons frequently alters TF occupancy Summary and perspective 7

8 Approximately 14% of all human coding bases contact a TF in at least one cell type (average 1.1% per cell type), 86.9% of genes contained coding TF footprints (average 33% per cell type) The density of TF footprints at different genic positions varied widely. Method: deoxyribonuclease Ⅰ (DNase Ⅰ ) footprinting Materials: 81 diverse cell types (human gnome)

9 SNV: single nucleotide variation Estimated mutational age at all (gray), synonymous (brown), and nonsynonymous (red) coding SNVs within and outside footprints. Both synonymous and nonsynonymous mutations within coding footprints were significantly younger than those outside of footprints.

10 Fourfold-degenerate bases: A position of a codon is said to be a fourfold degenerate site if any nucleotide at this position specifies the same amino acid. TFs constrain both codon choice (via constraint on 4FDBs) and amino acid choice (via NDBs) encoded at their recognition sites.

Introduction – Regulatory codes – “Duons” – Genomic footprint TFs densely populate and evolutionarily constrain protein-coding exons TFs modulate global codon biases Genetic variation in duons frequently alters TF occupancy Summary and perspective 11

12 For all amino acids encoded by two or more codons the codon that is preferentially used genome-wide is preferentially occupied by TFs. The third position of preferred codons overlapping footprints is under excess evolutionary constraint supports a general role for TFs in potentiating codon usage biases through the selective preservation of preferred codons.

Introduction – Regulatory codes – “Duons” – Genomic footprint TFs densely populate and evolutionarily constrain protein-coding exons TFs modulate global codon biases Genetic variation in duons frequently alters TF occupancy Summary and perspective 13

14 3% of coding footprints harbored heterozygous SNVs. 17.4% quantitatively skew the allelic origins of DNA fragments protected from cleavage by DNase Ⅰ in human cells, suggesting that such SNVs affect TF occupancy.

15 Such SNVs (mentioned before) are not biased toward whether they result in synonymous or nonsynonymous changes. Intriguingly, a large fraction of nonsynonymous variants are predicted not to alter protein function. This indicates that some variants within duons might primarily affect transcription factor binding instead. This supports the emerging idea that SNVs within protein-coding regions can lead to disease without affecting protein structure or function. Weatheritt, R J.; Badu, M M. Sceicne. 2013, 342: Proportion of SNVs in duons that allelically alter TF occupancy

Introduction – Regulatory codes – “Duons” – Genomic footprint TFs densely populate and evolutionarily constrain protein-coding exons TFs modulate global codon biases Genetic variation in duons frequently alters TF occupancy Summary and perspective 16

~14% regions called “duons” of the codons encode two types of information. The requirement for transcription factors to bind within protein-coding regions of the genome has led to a considerable bias in codon usage and choice of amino acids, in a manner that is constrained by the binding motif of each transcription factor. TFs modulate global codon biases 17.4% quantitatively SNVs those skew the allelic origins of DNA fragments affect transcription factor occupancy. Some SNVs within duons might primarily affect transcription factor binding instead. This supports the emerging idea that single-nucleotide variants within protein-coding regions can lead to disease without affecting protein structure or function. 17 It is unclear how the binding of a TF within protein-coding regions mechanistically influences the expression of a gene. It is also unclear whether binding of a TF within a protein-coding region may not directly affect gene expression but instead determine the formation and maintenance of higher-order chromatin structure.

19 Method: deoxyribonuclease Ⅰ (DNase Ⅰ ) footprinting Materials: 81 diverse cell types (human gnome) Stergachis, A J.; et al. Sceicne. 2013, 342:

20 A subset of TFs selectively avoid coding sequences. TFs involved in positioning the transcriptional preinitiation complex, such as NFYA and SP1, preferentially avoid the translated region of the first coding exon and typically occupy elements immediately upstream of the methionine start codon. Conversely, TFs involved in modulating promoter activity, such as YY1 and NRSF, preferentially occupy the translated region of the first coding exon (Fig. 3, A and C) (30, 31). These findings indicate that the translated portion of the first coding exon may serve functionally as an extension of the canonical promoter.

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