From: Analysis of the basal chordate Botryllus schlosseri reveals a set of genes associated with fertility
DE at Stage(s) of Blastogenesis | EST 5-11 contig name | Homo sapiens or Ascidian homologue | BaseMean Infertile | BaseMean Fertile | FoldChange | pval | padj | Function or Expression | Reference |
---|---|---|---|---|---|---|---|---|---|
A1*, A2, B1, C2 and D | CAP3_round1_contig_7511 | Histone H1.0 | 5.33 | 5031.92 | 944.26 | 1.15E-09 | 3.39E-07 | Regulates gene transcription through chromatin remodeling, facilitating expression of fertility-related genes. | [49] |
A1, B1*, B2, C1, C2 and D | CAP3_round1_contig_5534 | Vitellogenin-1 | 49.17 | 45603.55 | 927.44 | 2.26E-15 | 4.49E-12 | Involved in secretion of nutrients into the oocyte by follicle cells | |
A1*, B1, and B2 | Bot_c25439 | F-box only protein 24 isoform 3 | 1.18 | 1062.39 | 901.21 | 1.58E-19 | 1.23E-15 | Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex | [50] |
A1 and B1* | Bot_rep_c36004 | Erythrocyte band 7 integral membrane protein isoform a | 2.78 | 1395.43 | 502.30 | 4.21E-19 | 1.64E-15 | Expressed on red blood cells. | [51] |
A1 and B1* | Bot_rep_c36244 | Testis-specific serine/threonine-protein kinase 2 | 0.72 | 333.98 | 462.92 | 1.59E-15 | 3.11E-12 | Expressed in both mouse and human sperm. | [52] |
C2* | Bot_c1378 | Microfibrillar-associated protein 4 | 4.24 | 1334.72 | 314.97 | 1.84E-06 | 3.61E-03 | Involved in photoprotection of the skin. | [53] |
A1*, B1 and B2 | Bot_c2674 | Kelch-like protein 10 | 3.42 | 766.95 | 223.81 | 5.53E-04 | 1.41E-01 | Encodes a component of intercellular bridges in Drosophila egg chambers. | [54] |
A1, A2, B1*, and B2 | CAP3_round1_contig_5576 | Histone H2B type 1-L | 3.98 | 1152.34 | 289.37 | 7.74E-15 | 1.10E-11 | Required to condense chromatin in sperm, removes heterochromatin marks, facilitating gene expression | [55] |
A1, A2, B1* and B2 | Bot_rep_c35370 | Creatine kinase S-type mitochondrial | 7.80 | 2193.66 | 281.17 | 4.12E-18 | 1.38E-14 | Is expressed in cardiac and striated muscle. | [56] |
A1*, B1 and D | Bot_c3513 | Tolloid-likeprotein 1 | 0.61 | 159.21 | 261.65 | 2.42E-08 | 5.34E-06 | Mammalian tolloid (BMP-1) is a proteinase involved in ovarian tissue remodeling | [35] |
A1*, A2, B1 and B2 | Bot_rep_c45338 | Testis-specific serine/threonine-protein kinase 1 | 6.67 | 1358.25 | 203.49 | 4.31E-16 | 1.34E-12 | Testicular germ cell-specific expression, possible role at and after the meiotic phase of spermatogenesis | [26], 57] |
A1, B1, B2*, C2 and D | Bot_rep_c45532 | Low density lipoprotein-related protein 1 | 5.68 | 1129.89 | 199.07 | 3.26E-10 | 2.18E-06 | Mediates endocytosis of cholesterol-rich LDL. In mice, LDLR is expressed in germ cells | [58] |
B1, B2 and C2* | Bot_c16824 | Zona Pellucida sperm binding protein-1 | 2.88 | 568.93 | 197.42 | 2.72E-06 | 4.70E-03 | Involved in oocyte development, protection, sperm binding. | [33],59] |
A1, A2, B1* and D | Bot_c13044 | P-Selectin | 1.89 | 362.01 | 191.12 | 9.33E-11 | 4.21E-08 | Expressed in the oolema of oocytes in hamsters and humans, as well as in sperm following the acrosomal reaction | |
A1 and B1* | CAP3_round1_contig_8583 | Ubiquitin-conjugating enzyme E2 R2 | 10.47 | 1902.72 | 181.78 | 1.04E-11 | 6.27E-09 | Ubiquitin-protein ligase complex, mediates ubiquitination and proteosomal degradation of target proteins during spermatogenesis | [60] |
A1 and B1* | Bot_c2928 | NAD+-specific isocitrate dehydrogenase beta precursor | 7.87 | 1072.58 | 136.14 | 1.78E-05 | 2.23E-03 | Possible role in oxidation of isocitrate to alpha-ketoglutarate in the citric acid cycle. | [61] |
A1* and B1 | Bot_rep_c45410 | Outer dense fiber of sperm tails 3-like 2 | 5.51 | 750.03 | 135.99 | 3.47E-14 | 3.69E-11 | Structural protein surrounding the axoneme in both the middle piece and principal piece of the sperm tail. | [62] |
A1* and B1 | Bot_c16543 | CD81 antigen (Tetraspanin-8) | 1.19 | 150.88 | 125.95 | 2.73E-10 | 9.77E-08 | Expressed by granulosa cells surrounding the oocyte in mice. Reduced fertility in CD81-/- null mice, possible role in acrosomal reaction | [63] |
A1*, B1, B2 | CAP3_round1_contig_7986 | Meltrin-S | 5.49 | 625.35 | 113.78 | 1.78E-13 | 1.74E-10 | Mediates cleavage of proteoglycans during the release of the oocyte in mammals | [64] |
A1, B1* | CAP3_round1_contig_6892 | ADAM metallopeptidase domain 12 | 35.70 | 3526.16 | 98.75 | 1.55E-09 | 5.14E-07 | ADAMs play roles in spermatogenesis and sperm function, potentially by effecting maturation of sperm and their adhesion and migration | [64, 65] |
A1, A2*, and B1 | CAP3_round1_contig_4222 | Cyclin A1 | 8.29 | 808.46 | 97.45 | 4.87E-05 | 3.39E-02 | Involved in cell cycle. | [66] |
A1 and B1* | Bot_rep_c35625 | Serine racemase | 14.60 | 1226.71 | 84.00 | 1.37E-13 | 1.37E-10 | Expressed in human testes,pecifically in spermatogonia, spermatocytes, spermatids, Leydig and Sertoli cells | [67] |
A1, B1*, B2 | CAP3_round1_contig_4558 | Fibrous sheath-interacting protein 2 | 29.98 | 2389.31 | 79.67 | 3.66E-11 | 1.90E-08 | Expressed in late spermatocyte development. | [68] |
A1*, B1 and D | Bot_c1197 | Hemicentin-1 precursor | 22.88 | 1722.58 | 75.28 | 4.39E-13 | 3.55E-10 | Facilitates the gliding of the developing gonad along epithelial basement membranes and germline cellularization. | [69] |
A1*, A2 and B1 | CAP3_round1_contig_9899 | Testis-specific serine/threonine-protein kinase 6 | 21.59 | 1245.79 | 57.70 | 5.29E-12 | 3.18E-09 | Essential for spem production and function | [70] |
A1*, B1 and D | CAP3_round1_contig_9042 | OTOA protein | 91.00 | 4925.43 | 54.12 | 2.39E-12 | 1.54E-09 | Expressed in sensory epithelia of the inner ear.t Has also been classified as a testis-selective cancer/testis (CT) gene | [27] |
A1, A2, B1*, C2 and D | Bot_rep_c50436 | Fukutin | 21.63 | 1124.36 | 51.99 | 6.28E-06 | 8.64E-04 | Mouse homozygous-null embryos showed folding of the egg cylinder, leakage of maternal red blood cells into the yolk sac cavity. | [71] |
A1*, A2 and D | Bot_c2465 | ATP-binding cassette sub-family B member 5 isoform 1 | 59.69 | 2393.08 | 40.10 | 5.75E-11 | 2.56E-08 | In Drosophila, ABC transporters efflux prenylated peptides out of somatic gonadal precursors to serve as chemoattractants for migrating germ cells | [72] |
A2* | Bot_c25254 | Retinol dehydrogenase 12 | 37.74 | 1127.87 | 29.88 | 2.41E-08 | 1.87E-04 | In Botryllus schlosseri retinoic acid signaling is involved in gonad formation | [23] |
A1, B1* and D | CAP3_round1_contig_9460 | Tubulin beta-4B chain | 351.41 | 10282.63 | 29.26 | 1.61E-07 | 3.41E-05 | Tubulin is the major constituent of microtubules; post-translational modification bu monoglycalation specifi incorporation into axonemes. | [73] |
A1 and B1* | CAP3_round1_contig_2349 | Ciliary dynein heavy chain 9 | 122.18 | 3015.52 | 24.68 | 1.06E-08 | 3.02E-06 | Possible role in sperm development or motility | [74] |
A1*, A2, B1 and D | Bot_rep_c36144 | Cyclic nucleotide-gated olfactory channel | 46.02 | 1050.24 | 22.82 | 7.82E-09 | 1.91E-06 | Expressed in the flagellum of mature sperm, involved in sperm movement | [75] |
A1* | CAP3_round1_contig_7272 | Cyclin B3 | 280.56 | 1503.78 | 5.36 | 5.99E-04 | 5.22E-02 | Involved in cell cycle regulation | [66] |