1. Young Leaf Shoot Tip Axillary Bud Node Internode

2. Phytomere Node Leaf Axillary Bud Internode

3. Node Increase in length of the stem occurs largely by internodal elongation.

4. Plant cells are surrounded by rigid cell walls. Cell migration does not occur in plants.

5. Cell expansion plays a major role in growth Root cells expand their volume 50 times by expanding lengthwise but not widthwise

6. In roots, cell expansion plays a major role in growth Two competing plant hormones determine the direction of cell expansion: GA (gibberellic acid) promotes growth along the length Ethylene promotes growth along the width

7. Auxin and Cytokinin control shoot and root growth High levels of Cytokinin and low levels of Auxin promote shoot development (stems with leaves) High levels of Auxin and low levels of Cytokinin promote root development

8. The Miller-Skoog Experiment: Cloning 1.Place single cell on medium with high levels of Cytokinin and low levels of Auxin to promote shoot development (stems with leaves) 2.Place shoots on medium with high levels of Auxin and low levels of Cytokinin to promote root development at the base of the shoot 3.Transfer rooted shoots to soil and grow plants to maturity

9. Figure 38.2 Review of an idealized flower

10. Fertilization

11. Figure 38.10 The development of a dicot plant embryo

12. Pollination is the first step of the fertilization process.

13. The pollen “germinates” and grows down into the ovary where fertilization of the egg occurs.

14. A successful fertilization will produce a fertilized egg with 2X DNA.

15. Even at this one cell stage the embryo reveals polarity. The first cell division is asymmetric, producing a small apical cell and a larger basal cell.

16. The apical cell will later give rise to the entire “embryo proper”. The basal cell will give rise to a small umbilical cord-like structure called the suspensor.

17. The small apical cell divides several times to generate the globular embryo. All cells of this embryo appear morphologically similar.

18. Several divisions later morphological asymmetry is seen in the heart shaped embryo.

19. Arabidopsis embryogenesis

21. Cotyledons (seed leaves) Shoot Apical Meristem Hypocotyl (seedling stem) Root Root Apical Meristem

22. Plant Stem Cells: Shoot and root meristem Weigel and Jürgens, 2002; Bowman and Eshed, 2000; Nakajima and Benfey, 2002

23. - located at the tips of growing shoots What is a shoot apical meristem? -a group of undifferentiated “stem” cells -renew themselves while generating lateral organs off the flanks - 3 types:vegetative, inflorescence, floral

24. Gerd Jurgens searched for embryo pattern mutants. 1.Soak seeds in a mutagen 2.Grow plants to maturity These plants would be carriers of mutations (m/+) 3.When these carriers self-fertilize, the resulting embryos would be: +/+, m/+, m/m Mutants similar to gap mutants in flies, lacking regions of the embryo, including the apical structures, the stem (hypocotyl) and root, were identified

25. Embryo Pattern Mutants

26. Organization of the SAM Fletcher 2003

27. L1 and L2 cells divide anticlinally: perpendicular to the surface These divisions contribute to surface growth without increasing the number of cell layers

28. L3 cells, or corpus layers, divide in both planes to add additional cell layers to the shoot.

29. Organization of the SAM Fletcher 2003

30. Shoot Apical Meristem The shoot apical meristem can be divided into distinct zones.

31. Shoot Apical Meristem -stem cells The central zone is maintained as a pool of undifferentiated stem cells.

32. Shoot Apical Meristem -peripheral zone The peripheral zone is the site of organ initiation.

33. Shoot Apical Meristem -stem cells-peripheral zone As cell divisions occur in the central zone, the resulting cells are pushed into the peripheral zone where they are incorporated into organ primordia.

34. Dividing Stem Cells are Pushed into the Peripheral Zone

35. Shoot Apical Meristem -stem cells-peripheral zone The central zone cells will give rise to all of the above-ground organs of the mature plant.

36. Shoot Apical Meristem -stem cells-peripheral zone How is the stem cell population maintained throughout the life of the plant?

37. Shoot Apical Meristem -stem cells-peripheral zone A feedback loop between organ initiation and the stem cell population regulates the size of the meristem.

38. WUSCHEL and SHOOTMERISTEMLESS mutants fail to develop a shoot apical meristem. Genes Controlling Meristem Development Normal heart- stage embryo WUS or STM mutant embryo

39. STM and WUS mutants do not form a shoot apical meristem

40. CLAVATA1 and CLAVATA3 mutants develop a greatly enlarged shoot apical meristem. Genes Controlling Meristem Development Normal heart- stage embryo WUS or STM mutant embryo CLV1 or CLV3 mutant embryo

41. CLV1 mutants have a larger meristem and make more stem cells wt clv1

42. Fletcher et al., 1999 clv3 mutants make more stem cells and resemble clv1 mutants

43. STM and WUS are required to form and maintain the stem cell population Genes Controlling Meristem Development

44. STM and WUS are required to form and maintain the stem cell population CLV1 and CLV3 are required to prevent the over- proliferation of the undifferentiated stem cell population Genes Controlling Meristem Development

45. STM and WUS are homeobox genes and encode proteins that function as transcription factors Genes Controlling Meristem Development

46. STM and WUS are homeobox genes and encode proteins that function as transcription factors CLV1 encodes a receptor protein Genes Controlling Meristem Development

47. STM and WUS are homeobox genes and encode proteins that function as transcription factors CLV1 encodes a receptor protein CLV3 encodes a small protein that functions as a signaling molecule that binds to the CLV1 receptor Genes Controlling Meristem Development

48. CLV / WUS Interactions CLV3 is expressed in the L1 and L2 cell layers of the central zone

49. CLV / WUS Interactions CLV1 and WUS are expressed in a small domain of L3 cells in the central zone

50. CLV / WUS Interactions CLV3 expression is lost in WUS mutants. Therefore, WUS activates CLV3 expression.

51. CLV / WUS Interactions The expression domain of WUS is greatly enlarged in CLV1 and CLV3 mutants. Therefore, CLV1 and CLV3 negatively regulate (repress) WUS expression.

52. CLV / WUS Interactions CLV3 binds to and activates the CLV1 receptor, which then represses WUS expression.

53. CLV / WUS Interactions WUS is part of an “organizing center” that promotes stem cell proliferation in overlying cells.

54. CLV / WUS Interactions A feedback loop between CLV and WUS maintains the stem cell population throughout the life of a plant.

55. The greatly enlarged meristems that form in clv mutants are largely suppressed when the activity of STM is reduced (for example, in stm/+ plants). Genetic Interactions between STM and CLV

56. The greatly enlarged meristems that form in clv mutants are largely suppressed when the activity of STM is reduced (for example, in stm/+ plants). Similarly, the loss of shoot meristems in stm mutants is restored in plants that have reduced CLV activity (for example in clv/+ plants). Genetic Interactions between STM and CLV