H human and mouse with p-values below 0.05 are listed in supplemental

H human and mouse with p-values below 0.05 are listed in supplemental tables S2 and S3. In the human, the term system development is the term with the lowest p-value. This term is associated with 15 out of the 38 human imprinted genes. This corresponds to a 2.6 fold enrichment in comparison to the annotation frequency in the group of all genes. Cellular processes is the term which is associated with the largest number of imprinted genes in the human: 32 imprinted genes (84.2 of all imprinted genes) are associated with this term, whereas this is only the case for 74.6 of all genes. For comparison, the imprinted genes in mouse showed a narrower range of 1.8 and 2 fold enrichment for these two broad terms, and only for system development the Chebulagic acid web p-value is below 0.05. As shown in Table 1, only the five generic GO terms, multicellular organismal development, developmental process, neuron development, system development, and anatomical structure development appear in both species with close to 2-fold enrichment (p,0.05, Fisher exact test). Only neuron development is 5-fold enriched. As terms such as system development and cellular processes are rather general terms, we subsequently analyzed the enrichment of terms in the GO_FAT section of the DAVID database. This manually curated section contains only terms that are related to rather specific functions. As shown in Figure 1, among the enriched specific terms in human and mouse, some are linked to neurondevelopment and differentiation and are intimately related with the CDKN1C and NDN genes. Interestingly, the terms regulation of RNA metabolic process, regulation of transcription, DNA-dependent, and regulation of transcription are the terms that are associated with the largest numbers of human imprinted genes (28.9, 28.9 and 34.2 , respectively). Moreover, around 8.5 and 10.5 of the examined mouse imprinted genes are involved in the regulation process of phosphorylation and positive regulation of molecular function, respectively. This group includes the imprinted genes Igf2, Ins2, Kcnq1, Htr2a, Grb10, Ndn, Tp73, Impact, Cdkn1c, Zim2, and Plagl1. The two GO terms Regulation of RNA metabolic process and the daughter node Regulation of transcription, DNA-dependent are associated with processes involved in the role of RNA synthesis regulation. Some of the encoded proteins are tumor proteins; others are inhibitors of the cell cycle, thus inhibiting division. It is also worth mentioning that the functional term regulation of gene KS-176 web expression by genetic 1326631 imprinting (this is abbreviated to `genetic imprinting’ in the DAVID database) is over-represented as well and is associated with the genes INS, IGF2, and KCNQ1 (Note: INS and IGF2 are being interpreted by DAVID as a single locus that includes two alternatively spliced read-through transcript variants and align to the INS gene in the 59 region and to the IGF2 gene in the 39 region). These functional associations of IGF2 and KCNQ1 rely on publications reporting how a differentially methylated region in KCNQ1 controls imprinted expression of other genes in the neighborhood [17] and about epigenetic abnormalities in the IGF2/H19 region of Beckwith-Wiedemann syndrome patients [18]. Note that being associated with the GO term regulation of gene expression by genetic imprinting therefore does not refer to the “property” of the respective gene to be an imprinted gene itself but indeed whether it exerts regulatory function on other genes via genetic imprint.H human and mouse with p-values below 0.05 are listed in supplemental tables S2 and S3. In the human, the term system development is the term with the lowest p-value. This term is associated with 15 out of the 38 human imprinted genes. This corresponds to a 2.6 fold enrichment in comparison to the annotation frequency in the group of all genes. Cellular processes is the term which is associated with the largest number of imprinted genes in the human: 32 imprinted genes (84.2 of all imprinted genes) are associated with this term, whereas this is only the case for 74.6 of all genes. For comparison, the imprinted genes in mouse showed a narrower range of 1.8 and 2 fold enrichment for these two broad terms, and only for system development the p-value is below 0.05. As shown in Table 1, only the five generic GO terms, multicellular organismal development, developmental process, neuron development, system development, and anatomical structure development appear in both species with close to 2-fold enrichment (p,0.05, Fisher exact test). Only neuron development is 5-fold enriched. As terms such as system development and cellular processes are rather general terms, we subsequently analyzed the enrichment of terms in the GO_FAT section of the DAVID database. This manually curated section contains only terms that are related to rather specific functions. As shown in Figure 1, among the enriched specific terms in human and mouse, some are linked to neurondevelopment and differentiation and are intimately related with the CDKN1C and NDN genes. Interestingly, the terms regulation of RNA metabolic process, regulation of transcription, DNA-dependent, and regulation of transcription are the terms that are associated with the largest numbers of human imprinted genes (28.9, 28.9 and 34.2 , respectively). Moreover, around 8.5 and 10.5 of the examined mouse imprinted genes are involved in the regulation process of phosphorylation and positive regulation of molecular function, respectively. This group includes the imprinted genes Igf2, Ins2, Kcnq1, Htr2a, Grb10, Ndn, Tp73, Impact, Cdkn1c, Zim2, and Plagl1. The two GO terms Regulation of RNA metabolic process and the daughter node Regulation of transcription, DNA-dependent are associated with processes involved in the role of RNA synthesis regulation. Some of the encoded proteins are tumor proteins; others are inhibitors of the cell cycle, thus inhibiting division. It is also worth mentioning that the functional term regulation of gene expression by genetic 1326631 imprinting (this is abbreviated to `genetic imprinting’ in the DAVID database) is over-represented as well and is associated with the genes INS, IGF2, and KCNQ1 (Note: INS and IGF2 are being interpreted by DAVID as a single locus that includes two alternatively spliced read-through transcript variants and align to the INS gene in the 59 region and to the IGF2 gene in the 39 region). These functional associations of IGF2 and KCNQ1 rely on publications reporting how a differentially methylated region in KCNQ1 controls imprinted expression of other genes in the neighborhood [17] and about epigenetic abnormalities in the IGF2/H19 region of Beckwith-Wiedemann syndrome patients [18]. Note that being associated with the GO term regulation of gene expression by genetic imprinting therefore does not refer to the “property” of the respective gene to be an imprinted gene itself but indeed whether it exerts regulatory function on other genes via genetic imprint.