Basic Leucine Zipper and W2 Domain-Containing Protein 2 is a protein that is encoded by the BZW2gene.[5][6] It is a eukaryotic translation factor[vague] found in species up to bacteria. In animals, it is localized in the cytoplasm and expressed ubiquitously throughout the body. The heart, placenta, skeletal muscle, and hippocampus show higher expression. In various cancers, upregulation tends to lead to higher severity and mortality. It has been found to interact with SARS-CoV-2.
Gene
BZW2 is known as Basic Leucine Zipper W2 Domain-Containing Protein 2, MST017, MSTP017, 5MP1, Eukaryotic Translation Factor 5, and HSPC028.[7] It is located on chromosome 7 at p21.1 on the plus strand. The gene spans 60,389 base pairs, at coordinates 16,583,248 – 16,804,999. There are 12 exons.
Protein
There are two known isoforms of BZW2. Isoform 1 is 419 amino acids long and is the most abundant form. Isoform 2 is 225 amino acids, containing only 11 exons and a shorter N-terminus.[7]
The coded protein is 419 amino acids long and weighs 48.3 kDa.[8] As described in the name, the protein contains a leucine-zipper motif. Four “L……” repeats are present in the beginning, giving rise to the characteristic leucine zipper helix within the 3D structure. An eIF5C domain follows the leucine motif, which is a part of proteins that are important for strict regulation of cellular processes.[9]
The amino acid composition of BZW2 has a higher amount of lysines and a lower amount of prolines in humans but a higher glutamic acid composition in its orthologs.[10] The human BZW2 protein has an overall charge of -3 which can go down to -9 in orthologs. There are no significant charge clusters. There is also a KELQ repeat that has remained conserved in animals.
Sequence of BZW2 is shown with positions of spacing information, charge clusters, and repeats.
The secondary structure contains a majority of alpha helices.[11] There are 19 alpha helices in all orthologs, except for two additional beta sheets which are absent in humans. The tertiary structure forms a repeated fold of alpha-helices, a structure that is conserved through bacteria.
BZW2 structure from Phyre2 colored from N-terminus (red) to C-terminus (blue).
Regulation
Gene-level
There are three known promoters for BZW2.[12] It is regulated by numerous transcription factors, including an estrogen receptor transcription factor (ESR2, ES3), leucine zipper transcription factor (RRFIP1), and Y sex-determining transcription factors (SRY). With these transcription factors, BZW2 has regulated expression in organs that contribute to cellular functions. The Y sex-determining transcription factor works to regulate BZW2 expression in the testis. Throughout the body, BZW2 is ubiquitously expressed within tissues. There is elevated mRNA abundance in the heart, placenta, and skeletal muscle.
Transcript-level
There are four major stem loops in the 5’ untranslated and four in the 3’ untranslated region that function in transcript-level regulation.[13]
Schematic of the post-translational modification locations on the BZW2 protein.
Evolution
BZW2 has a single paralog, BZW1 which is conserved up to plants.[15] There are BZW2 orthologs up to a couple species of bacteria. The most distant ortholog was Microbacterium arborescens. BZW2 contains an eIF5C domain which is also present in eIF2BE, eIF4G, eIF5, and a GAP protein specific for eIF2.[16]
Select BZW2 Orthologs
Species
Common Name
Order
Million years since divergence from humans
Similarity %
Identity %
Homo sapiens
Human
Primates
0
100
100
Mus musculus
Mouse
Rodentia
29
100
99
Phocoena sinus
Vaquita
Artiodactyla
94
99
99
Ornithorhynchus anatinus
Duckbill platypus
Monotremata
180
97
95
Columba livia
Rock pigeon
Columbiformes
318
95
90
Pantherophis guttatus
Corn snake
Squamata
318
97
92
Terrapene carolina triunguis
Three-toed box turtle
Testudines
318
97
92
Pygoscelis adeliae
Adelie penguin
Spehnisciformes
318
96
97
Xenopus tropicalis
Western clawed frog
Anura
419
97
90
Danio rerio
Zebrafish
Cypriniformes
433
84
95
Ambylraia radiata
Thorny skate
Raiiformes
465
96
86
Petromyzon marinus
Sea lamprey
Petromyzontiformes
599
86
73
Acanthaster planci
Crown-of-thorns starfish
Valvatida
627
69
51
Drosophila melanogaster
Fruit fly
Diptera
736
72
49
Coptotermes formosanus
Formosan termite
Blattodea
736
69
51
Gigaspora rosea
NA
Diversisporales
1017
62
38
Rhizophagus irregularis
NA
Glomerales
1017
62
38
Camellia sinensis
Tea plant
Ericales
1275
55
35
Rhodamnia argentea
Malletwood
Myrtales
1275
69
47
Microbacterium arborescens
NA
Actinomycetales
4090
30
20
Leptospira ognonensis
NA
Leptospirales
4090
51
37
Aeromonas veronii
NA
Aeromondales
4090
87
69
A phylogenetic tree illustrates the BZW2 sequence relationships between orthologs.
Compared to Cytochrome C, a quickly diverging protein, and Fibrinogen, a slowly diverging protein, BZW2 has had slow corrected divergence over time, illustrating conservation and protein importance.
BZW2 corrected divergence over million years diverged from humans,
EIF2S2 and ORF4 work to synthesize and replicate BZW2.[17] PSTPIP1 and NEK4 are regulatory proteins that help in the functionality of BZW2.[18][19] SNW1, a spliceosome protein, splices BZW2 mRNA variants.[20] The protein rep is part of SARS-CoV-2 virus and inhibits translation of BZW2.[21]
Clinical significance
Cancer
BZW2 has been studied to determine its role in multiple cancers. Overall, the studies all showed that upregulation of BZW2 lead to more severe forms of cancer, higher rate of mortality, and increased likeliness of reoccurrence.
A 2019 study focused on the effect of BZW2 in colorectal cancer.[22] It found that upregulation of BZW2 promoted tumor growth and had a downstream upregulation effect on c-Myc, a proto-oncogene. A second study from 2020 determined this upregulation also had a positive effect on the activation of the ERK/MAPK pathway. [23]
^Huang L, Chen S, Fan H, Ai F, Sheng W (May 2020). "BZW2 promotes the malignant progression of colorectal cancer via activating the ERK/MAPK pathway". Journal of Cellular Physiology. 235 (5): 4834–4842. doi:10.1002/jcp.29361. PMID31643092. S2CID204850013.
^Jin X, Liao M, Zhang L, Yang M, Zhao J (February 2019). "Role of the novel gene BZW2 in the development of hepatocellular carcinoma". Journal of Cellular Physiology. 234 (9): 16592–16600. doi:10.1002/jcp.28331. PMID30805927. S2CID73473337.