Consequences of knocking out BMP signaling in the mouse

Genesis - Tập 35 Số 1 - Trang 43-56 - 2003
Guang‐Quan Zhao1
1Cecil H. & Ida Green Center for Reproductive Biology Sciences, Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Texas

Tóm tắt

Abstract

Summary: During the past two decades, a significant amount of data has been accumulated revealing the intriguing functions of bone morphogenetic proteins (BMPs) in all aspects of embryonic development and organogenesis. Numerous genes encoding BMPs, BMP receptors, and their downstream signal transducers have been mutated in the mouse through targeted mutagenesis. This review focuses on what is known about the role of BMP signaling in gastrulation, mesoderm formation, left–right asymmetry, neural patterning, skeletal and limb development, organogenesis, and gametogenesis as revealed by BMP‐signaling mutants. genesis 35:43–56, 2003. © 2002 Wiley‐Liss, Inc.

Từ khóa


Tài liệu tham khảo

Ahn K, 2001, BMPR‐IA signaling is required for the formation of the apical ectodermal ridge and dorsal‐ventral patterning of the limb, Development, 128, 4449, 10.1242/dev.128.22.4449

10.1038/12971

Bahamonde ME, 2001, BMP3: to be or not to be a BMP

10.1101/gad.13.23.3149

10.1242/dev.127.3.605

10.1016/S0092-8674(00)80560-7

10.1016/0092-8674(94)90251-8

10.1006/dbio.2000.9670

10.1038/35082103

10.1146/annurev.cellbio.17.1.87

10.1016/S0925-4773(01)00367-7

Chang H, 1999, Smad5 knockout mice die at mid‐gestation due to multiple embryonic and extraembryonic defects [In Process Citation], Development, 126, 1631, 10.1242/dev.126.8.1631

10.1006/dbio.1999.9594

10.1074/jbc.274.6.3672

10.1002/gene.10046

10.1038/381155a0

10.1242/dev.120.7.1919

10.1242/dev.126.3.535

10.1038/83810

10.1016/S0960-9822(96)00702-6

10.1210/endo.136.6.7750489

10.1242/dev.121.6.1845

10.1038/383531a0

10.1073/pnas.062010399

10.1210/mend.12.12.0206

10.1002/(SICI)1097-0177(199703)208:3<349::AID-AJA6>3.0.CO;2-I

10.1101/gad.9.22.2795

10.1006/dbio.1997.8664

10.1016/S0925-4773(97)00673-4

10.1002/(SICI)1097-4695(19990905)40:3<271::AID-NEU1>3.0.CO;2-C

10.1038/374464a0

10.1073/pnas.241508898

10.1101/gad.12.23.3764

10.1038/72835

10.1006/dbio.1998.9191

10.1073/pnas.042390499

10.1016/S0092-8674(00)81249-0

10.1002/jez.1401670202

10.1006/dbio.2000.0127

10.1101/gad.12.6.844

10.1242/dev.126.11.2551

10.1016/0092-8674(94)90319-0

10.1016/0092-8674(94)90320-4

10.1073/pnas.96.22.12595

10.1002/gene.10048

10.1101/gad.10.13.1580

Hogan B, 1994, Manipulating the mouse embryo: a laboratory manual

10.1016/S0092-8674(00)80134-8

10.1016/S0092-8674(00)81250-7

10.1002/gene.10059

10.1073/pnas.95.16.9337

Jackson SM, 1997, dally, a Drosophila glypican, controls cellular responses to the TGF‐beta‐related morphogen, Dpp, Development, 124, 4113, 10.1242/dev.124.20.4113

10.1006/excr.1996.3411

10.1210/en.131.6.2703

10.1210/en.132.1.477

10.1002/(SICI)1520-6408(1998)22:4<340::AID-DVG4>3.0.CO;2-6

10.1074/jbc.270.10.5625

10.1006/dbio.2001.0284

10.1006/dbio.1994.1300

10.1016/0092-8674(92)90510-J

10.1002/gene.10032

10.1074/jbc.M004649200

10.1101/gad.13.4.424

10.1006/dbio.2001.0469

10.1101/gad.12.21.3394

10.1128/MCB.15.7.3479

10.1242/dev.128.10.1831

10.1101/gad.9.22.2808

10.1006/dbio.2001.0334

10.1016/S0092-8674(00)81817-6

10.1074/jbc.273.40.25628

10.1016/0925-4773(94)00295-X

10.1016/S0092-8674(00)81296-9

10.1016/S0303-7207(99)00241-5

10.1038/360313a0

10.1038/374356a0

10.1038/374354a0

10.1210/me.9.1.131

10.1038/387083a0

10.1038/10320

10.1046/j.1365-2443.1997.1400338.x

10.1016/S0092-8674(00)81472-5

10.1016/S1097-2765(00)80331-7

10.1016/S1534-5807(01)00006-5

10.1101/gad.9.24.3027

10.1101/gad.10.20.2577

10.1006/dbio.1999.9378

10.1002/gene.10038

10.1172/JCI8256

10.1016/0092-8674(94)90293-3

10.1016/S0092-8674(00)81769-9

10.1038/31693

10.1101/gad.11.14.1812

10.1073/pnas.97.6.2626

10.1006/dbio.1996.0259

10.1006/dbio.2000.9831

10.1016/S0092-8674(00)80132-4

10.1152/ajprenal.1997.273.6.F961

10.1242/dev.126.5.883

10.1038/ng1295-409

10.1002/(SICI)1097-0177(200002)217:2<146::AID-DVDY2>3.0.CO;2-I

10.1093/genetics/139.1.241

10.1038/73472

10.1073/pnas.92.26.12141

10.1101/gad.201801

10.1016/0092-8674(95)90292-9

10.1242/dev.124.13.2659

10.1038/376333a0

10.1073/pnas.93.2.790

10.1016/S0925-4773(99)00311-1

10.1093/genetics/139.3.1347

10.1006/dbio.2001.0244

10.1038/359693a0

10.1101/gad.12.1.107

Solloway MJ, 1999, Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup, Development, 126, 1753, 10.1242/dev.126.8.1753

10.1002/(SICI)1520-6408(1998)22:4<321::AID-DVG3>3.0.CO;2-8

10.1006/dbio.1999.9370

10.1038/35047564

10.1242/dev.122.12.3969

10.1038/368639a0

10.1073/pnas.91.22.10255

10.1016/S0092-8674(00)81132-0

10.1016/S0955-0674(96)80058-5

10.1242/dev.127.14.3079

Tremblay KD, 2001, Mouse embryos lacking Smad1 signals display defects in extra‐embryonic tissues and germ cell formation, Development, 128, 3609, 10.1242/dev.128.18.3609

10.1007/BF02152373

10.1007/BF02563992

Urist MR, 1976, A bone morphogenetic polypeptide, Calcif Tissue Res, 21, 81, 10.1007/BF02546432

10.1073/pnas.76.4.1828

10.1242/dev.124.5.1033

10.1101/gad.8.4.414

10.1016/S0092-8674(00)81407-5

10.1006/dbio.1998.9153

10.1073/pnas.95.16.9378

10.1002/j.1460-2075.1996.tb00358.x

10.1038/376331a0

10.1095/biolreprod64.4.1225

10.1101/gad.9.17.2105

10.1016/0092-8674(92)90395-S

10.1038/370341a0

10.1006/bbrc.1995.1958

10.1038/sj.onc.1203504

10.1210/mend.15.6.0662

10.1073/pnas.95.7.3667

Yang X, 1999, Angiogenesis defects and mesenchymal apoptosis in mice lacking SMAD5 [In Process Citation], Development, 126, 1571, 10.1242/dev.126.8.1571

10.1093/emboj/18.5.1280

10.1083/jcb.153.1.35

10.1002/gene.10029

10.1002/0470868732.ch15

10.1016/S1097-2765(01)00249-0

10.1242/dev.127.3.621

10.1073/pnas.141002798

10.1006/dbio.2001.0173

10.1210/mend.14.7.0479

10.1073/pnas.151242798

10.1242/dev.122.10.2977

10.1016/0925-4773(96)00543-6

10.1016/S0925-4773(96)00622-3

10.1101/gad.10.13.1657

10.1242/dev.125.6.1103

10.1006/dbio.2001.0448

10.1038/361543a0

10.1016/S0092-8674(00)81730-4

10.1016/S0092-8674(00)80133-6