Table 1. Literature based “legacy” genes provide a core to build a SS to PT development network.
Gene (Node) | Source |
Notch 1, 2 | [17], [21] |
RBPJ | [21] |
Hyaluronic Acid | [26] |
CD44 (HA receptor) | [26] |
RHAMM (HMMR, HA receptor) | [26] |
E-Cadherin (CDH1) | [27] |
ZO-1 (TJP1) | [27] |
Lim1 (LHX1) | [29] |
Brn1 (POU3F3)* | [30] |
Oat1 (SLC22A6) | [12] |
Oat3 (SLC22A8) | [12] |
Oct1 (SLC22A1) | [12] |
Oct2 (SLC 22A2) | [13] |
(SLC 47A1) | [13] |
(SLC 15A2) | [13] |
WT1 | [28] |
Jag1 | [17] |
Dll1 | [17] |
Hey1 | [22] |
Hes1 | [22], [23] |
Hnf1a | [24] |
Hnf4a | [25] |
Genes representing known regulators of nephron development and of proximal tubule function were used as the basis of the s-shaped body to proximal tubule stage specific network. This core of genes is the basis for addition of differentially expressed genes from in vitro and in vivo microarray experiments.
Brn1 is determinant of distal tubular development.