Hp53int1

Figure 1: The location of Hp53int1 protein on chromosome 17p.13, region 7,685,260 bp-7,686,371 bp

The Hp53int1 gene is located on chromosome 17p.13, encoded by a DNA sequence 1125 base pairs in length, covering region 7,685,260 bp-7,686,371 bp.[1] The Hp53int1 gene has two aliases, WRAP53int1 and TP53int1, in accordance to its overlap with the WRAP53 and TP53int1 genes on chromosome 17.[2] Hp53int1 is located downstream of the p53p2 start site.[3]

Hp53int1 does not have multiple exons, and therefore has no isoforms.

5' UTR Analysis[5]:The consensus folding of the 5’ UTR of Hp53int1. Two loops are formed from amino acids 1-9 and 12-21 respectively. The connecting amino acids of both loops are rich in G’s and C’s.

Hp53int1 is encoded by a polyadenylated transcript 1125 base pairs in length. There is a repeat sequence between base pairs 633…926 and a regulatory Poly A tail sequence between base pairs 496…1000.[1] The repeat sequence between base pairs 633 and 926 is noted to be similar to the Alu SC subfamily repeat, a sequence that characterizes the most abundant repeat sequences in humans and primates, and which likely diverged from other Alu subfamily complexes around 32 million years ago.[6]

The Hp53int1 protein has a molecular weight of 13.3 kdal and is 118 amino acids in length.[2][8] It is a basic protein.[8] There is one highly conserved amino acid sequence between 102-110.[9] Serine site distribution is significantly higher than Arginine and Tyrosine sites.[10] There is a possible Casein Kinase II phosphorylation site between amino acids 22-25.[11] Casein Kinase II phosphorylation is involved in cell proliferation. Three regions of disorder are predicted for the Hp53int1 protein.[10]

Web Logo[12] results using a multiple sequence alignment between Hp53int1 and its orthologs.

Post translational modifications

There is a possible O-ß-GlcNAc site between amino acids 14-20.[13] There are no transmembrane domains nor signal peptides.

There is a conserved phosphorylation site at S5, S15, and S20.[14]

Predictions for O-ß-GlcNAc in the Hp53int1 protein given by Yin O Yang.[13] The green bars represent the potential for O-ß-GlcNAc attachment sites in Hp53int1, and must reach a value > 0.50 to be considered a likely site. There is one predicted attachment site for Hp53int1.

There is low tissue specificity for the Hp53int1 gene.[18] When comparing various samples of adult human tissues there is high expression in the thymus, ovaries, lymph nodes, and white blood cells. There was a high expression score for both RNA expression and protein expression in proximal digestive tract, gastrointestinal tract, and male/female tissues. During fetal development between weeks 10 and 16, there is elevated expression in the lung and heart tissues.

Hp53int1 is differentially expressed under conditions that require cell proliferation or apoptosis, in accordance to its congruence with the TP53 tumor suppressor gene[19]

The Hp53int1 protein is likely involved in the regulation of cellular proliferation and apoptosis. This is indicated by the use of apoptosis-regulator and ubiquitination regulator interacting proteins, its share of transcription factors with TP53 (especially the SMAD2, SRY, and ETV7 transcription factors), its location downstream of the p53p2 start site, its casein kinase II phosphorylation site, and its ubiquitous expression across tissues. The Hp53int1 gene expression is increased in environments when proteins that reduce cell proliferation are overexpressed, suggesting its requirement in cellular environments that need to arrest cell growth.[19] Also, quantitative analysis shows that the general hp53 protein is absolutely required for the activation of cellular response to DNA damage.[22]

Interacting Proteins

The following interacting proteins[23] were found for TP53, but can be applied to Hp53int1 due to their chromosomal relationship. Important to note: the functions of these interacting proteins are directly involved in cell regulation (ubiquitination, transcriptional regulator, apoptosis, and protein-tyrosine kinase).

There is evidence that the Hp53int1 gene is involved in tumor suppression. Hp53int1 overlaps with TP53 exon 1 (TAD1).[24] Mutations within this region can result in alternative exon expression or incomplete splicing and a loss of tumor suppressor function. Regarding osteosarcoma, these rearrangements within TAD1 have been detected in ~20% of the cases involving incomplete splicing of TP53. These rearrangements are located across the full sequence of TP53 intron 1, but the majority of them will cluster in a domain of the Hp53int1 transcript, suggesting that these rearrangements may be facilitated by chromatin conformation within this locus[25]