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Vertebrate limbs Mouse forelimb 1 2 3 4 Anterior Proximal 2 Dorsal Posterior Chicken forelimb :Wing 4 3 Distal Ventral 5 Vertebrate limb patterning: Retrospection and Introspection From 2D to 3D 40 hrs. 60 hrs. 80 hrs. 100 hrs. Limb bud in 3.5 days old chick embryo Day 3 Day 3.5 Day 3 Day 3.5 The lateral plate mesoderm and overlying ectoderm is specified to form the limb buds. Day 3 The lateral plate mesoderm proliferates in the region where the limb buds develop. Day 3.5 The body wall folds over to close ventrally. Day 4 Vertebrate limbs From 2D to 3D 40 hrs. 60 hrs. 80 hrs. 100 hrs. Induction of limb bud Specification of limb bud Specification of limb bud RE-Specification of limb bud Nature. 1999 Apr 29;398(6730):814-8 Anterior Dorsal Posterior Distal Proximal Ventral D-V axis Dorsal Ventral { Wnt-7a r-fng Lateral plate mesoderm D V Lmx-1 Dorsal AER en-1 Lessons from D/V axis formation • Ectoderm specifies mesoderm • Ventral fate seems default • AER positioning and Dorsalization of mesoderm • Both dictated by en-1 • But are disconnected { Wnt-7a r-fng en-1 r-fng Wnt-7a Lmx-1 Dorsal Lmx-1 AER AER formation Dorsal pattern en-1 Apical Ectodermal Ridge A signaling center P/D axis and the AER Time of AER removal Early Intermediate Late Normal Resultant wing Progress zone model Lewis Wolpert, 1973 Schematic of X-irradiation of stage 19-21 limb buds No irradiation or low-dose Intermediate dose High dose Cell death and decreased cell proliferation are significant factors in phenotypes produced by AER removal. AER removed At stage 19 FGF at T0 FGF at T12 AER removed At stage 23 FGF at T0 FGF at T12 Nature. 2002 Aug 1;418(6897):539-44, Dudley AT, Ros MA, Tabin CJ. Descendents of cells in the early limb bud contribute to only one proximodistal segment. 100-200 μM 200-300 μM U 200-300 μM 100-200 μM U 100-200 μM Nature. 2002 Aug 1;418(6897):539-44, Dudley AT, Ros MA, Tabin CJ. Progressive specification model Dudley and Tabin, 2002 Progress zone Vs Progressive specification model Genes Dev. 2007 21: 1433-1442 FGFs are the signals from AER FGFs: Necessary and Sufficient for AER function A/P axis and ZPA Normal wing bud Normal wing 2 4 ZPA 3 A/P axis and ZPA Ectopic ZPA transplanted wing bud Ectopic ZPA transplanted wing 3 4 2 2 4 Retinoic acid bead implantation can also achieve this 3 ZPA and Sonic Hedgehog Shh is expressed at the ZPA Expression of Shh mRNA Riddle and Tabin, 1993 ZPA and Sonic Hedgehog Shh protein can substitute ZPA Ectopic Shh bead transplanted wing bud Ectopic Shh bead transplanted wing Shh protein soaked bead 3 4 2 2 4 3 Is Shh the real morphogen Is BMP2 the real morphogen acting downstream of Shh? Shh protein domain Shh mRNA domain BMP2 mRNA domain BMP4 does not cause patterning defect defect Combined loss of BMP2 and BMP7 Albeit combined loss of BMP2 and BMP4 causes severe skeletal defect Forelimb WT Hindlimb Bmp2c/c, Bmp7-/-, Bmp2c/c, Bmp4c/c, Prx1 cre Prx1 cre If not secondary morphogen then what? Expansion-based temporal gradient of Shh If not secondary morphogen then what? Expansion-based temporal gradient of Shh Supporting evidences : 1. Loss of Shh spares digit 1 => Shh independent 2. Delayed marking marks only digit 4 and 5 3. Non-diffusible Shh mutant only loses digits 2 and 3 4. Agrees with bead implantation studies Digit identity – Graded signal interpretation Randall D. Dahn and John F. Fallon* 21 JULY 2000 VOL 438 289 SCIENCE Posterior ID wins Randall D. Dahn and John F. Fallon* 21 JULY 2000 VOL 438 289 SCIENCE Stapled Not stapled Randall D. Dahn and John F. Fallon* 21 JULY 2000 VOL 438 289 SCIENCE Inter-digital mesenchyme specifies DIGIT identity Posterior ID prevails Modulation of ID BMP levels causes homeotic digital transformation BMP4 does not cause patterning defect defect Combined loss of BMP2 and BMP7 Albeit combined loss of BMP2 and BMP4 causes severe skeletal defect Forelimb WT Hindlimb Bmp2c/c, Bmp7-/-, Bmp2c/c, Bmp4c/c, Prx1 cre Prx1 cre Competence Vs permissibility Restriction of Shh expression domain 1. Retinoic acid can induce ectopic ZPA 2. Hoxb8 is expressed immediately following RA application ZPA cells or even flank cells (prior to Shh expression) if transplanted in the anterior margin can induce Shh. Retinoic acid bead implanted in the anterior promote Shh expression and ZPA activity. Why should not Shh be expressed in the anterior margin? Anterior necrotic zone OR Gli3 mediated repression? RA ----- Hoxb8--- Shh Gli3 Interaction between axes Competence to express Shh Retinoic acid bead implantation Non-AER D/V border : Another signaling center :: Regulates Tbx2 expression Non-AER D/V border is required to maintain Tbx2 expression Non-AER D/V ectoderm can induce ectopic Tbx2 expression Tbx2 is in red, anti-quail antibody QCPN is in green - Non-AER D/V ectoderm can induce ectopic Tbx2 expression Non-AER D/V border : Another signaling center :: Regulates Tbx2 expression => Upregulates Shh expression Shh expression upon non-AER D/V transplantation - Restricted to the posterior margin only Why is Tbx2 and Shh excluded from under AER? Rather Shh expression expands underneath the AER Dorsal ectoderm Wnt-7a, r-fng BMP FGF Ventral ectoderm en-1 Gremlin Dorsal ectoderm Wnt-7a, r-fng BMP FGF Ventral ectoderm en-1 Gremlin Way forward? • Reductionist approach • Build mini circuits • Construct predictive model • Experimental validation and revisiting the model