The making of gametes in higher plants

Higher plants have evolved to be one of the predominant life forms on this planet. A great deal of this evolutionary success relies in a very short gametophytic phase which underlies the sexual reproduction cycle. Sexual plant reproduction takes place in special organs of the flower. In most species the processes of gametogenesis, pollination, syngamy and embryogenesis are sequentially coordinated to give rise to a functional seed in a matter of few weeks. Any of these processes is so intricately complex and precisely regulated that it becomes no wonder that each involves more specific genes and cellular processes than any other function in the plant life cycle. While variability generation - the evolutionary output of the sexual cycle - is the same as in any other Kingdom, plants do it using a completely original set of mechanisms, many of which are not yet comprehended. In this paper, we cover the fundamental features of male and female gametogenesis. While the physiological and cellular bases of these processes have been continuously described since the early nineteen century, recent usage of Arabidopsis and other species as central models has brought about a great deal of specific information regarding their genetic regulation. Transcriptomics has recently enlarged the repertoire and pollen became the first gametophyte to have a fully described transcriptome in plants. We thus place special emphasis on the way this newly accumulated genetic and transcriptional information impacts our current understanding of the mechanisms of gametogenesis

Gametophyte interaction and sexual reproduction: how plants make a zygote

The evolutionary success of higher plants relies on a very short gametophytic phase, which underlies the sexual reproduction cycle. Sexual plant reproduction takes place in special organs of the flower: pollen, the male gametophyte, is released from the anthers and then adheres, grows and interacts along various tissues of the female organs, collectively known as the pistil. Finally, it fertilizes the female gametophyte, the embryo sac. Pollen is released as bi or tricellular, highly de-hydrated and presumably containing all the biochemical components and transcripts to germinate. Upon hydration on the female tissues, it develops a cytoplasmic extension, the pollen tube, which is one of the fastest growing cells in nature. Pollen is completely "ready-to-go", but despite this seemingly simple reaction, very complex interactions take place with the female tissues. In higher animals, genetic mechanisms for sex determination establish striking developmental differences between males and females. In contrast, most higher plant species develop both male and female structures within the same flower, allowing self-fertilization. Outcrossing is ensured by self-incompatibility mechanisms, which evolved under precise genetic control, controlling self-recognition and cell-to-cell interaction. Equally important is pollen selection along the female tissues, where interactions between different cell types with inherent signalling properties correspond to check-points to ensure fertilization. Last but not least, pollen-pistil interaction occurs in a way that enables the correct targeting of the pollen tubes to the receptive ovules. In this review, we cover the basic mechanisms underlying sexual plant reproduction, from the structural and cellular determinants, to the most recent genetic advances

Signalling by tips

New molecules, including protein kinases, lipids and molecules that have neurotransmitter activities in animals have emerged as important players in tip-growing cells. Transcriptomics analysis reveals that the largest single class of genes expressed in pollen tubes encode signal transducers, reflecting the necessity to decode complex and diverse pathways that are associated with tip growth. Many of these pathways may use common intracellular second messengers, with ions and reactive oxygen species emerging as two major common denominators in many of the processes involved in tip growth. These second messengers might influence the actin cytoskeleton through known interactions with actin-binding proteins. In turn, changes in the dynamic properties of the cytoskeleton would define the basic polarity events needed to shape and modify tip-growing cells

Investigation of Single Boron Acceptors at the Cleaved Si:B (111) Surface

The cleaved and (2 x 1) reconstructed (111) surface of p-type Si is investigated by scanning tunneling microscopy (STM). Single B acceptors are identified due to their characteristic voltage-dependent contrast which is explained by a local energetic shift of the electronic density of states caused by the Coulomb potential of the negatively charged acceptor. In addition, detailed analysis of the STM images shows that apparently one orbital is missing at the B site at sample voltages of 0.4 - 0.6 V, corresponding to the absence of a localized dangling-bond state. Scanning tunneling spectroscopy confirms a strongly altered density of states at the B atom due to the different electronic structure of B compared to Si.Comment: 6 pages, 7 figure

NMR Detection of Temperature-Dependent Magnetic Inhomogeneities in URu2Si2

We present 29Si-NMR relaxation and spectral data in URu2Si2. Our echo-decay experiments detect slowly fluctuating magnetic field gradients. In addition, we find that the echo-decay shape (time dependence) varies with temperature T and its rate behaves critically near the Neel temperature TN, indicating a correlation between the gradient fluctuations and the transition to small-moment order. T-dependent broadening contributions become visible below 100 Kelvin and saturate somewhat above TN, remaining saturated at lower temperatures. Together, the line width and shift suggest partial lattice distortions below TN. We propose an intrinsic minority phase below $T_{\rm N}$ and compare our results with one of the current theoretical models.Comment: 2 pages RevTeX, 1 figure, SCES 99-Japan, to appear in Physica

Antiferromagnetic ordering in the Kondo lattice system Yb2_2Fe3_3Si5_5

Compounds belonging to the R$_2$Fe$_3$Si$_5$ series exhibit unusual superconducting and magnetic properties. Although a number of studies have been made on the first reentrant antiferromagnet superconductor Tm$_2$Fe$_3$Si$_5$, the physical properties of Yb$_2$Fe$_3$Si$_5$ are largely unexplored. In this work, we attempt to provide a comprehensive study of bulk properties such as, resistivity, susceptibility and heat-capacity of a well characterized polycrystalline Yb$_2$Fe$_3$Si$_5$. Our measurements indicate that Yb$^{3+}$ moments order antiferromagnetically below 1.7 K. Moreover, the system behaves as a Kondo lattice with large Sommerfeld coefficient ($\gamma$) of 0.5~J/Yb mol K$^{2}$ at 0.3 K, which is well below T$_N$. The absence of superconductivity in Yb$_2$Fe$_3$Si$_5$ down to 0.3 K at ambient pressure is attributed to the presence of the Kondo effect.Comment: 10 pages, 3 figures, tex document. A fuller version has appeared in PRB. Here we have omitted the figures showing the crystal structure and the fitting of the X-ray pattern. Also the table with the lattice parameters obtained from fitting has been remove

Spin polarons in triangular antiferromagnets

The motion of a single hole in a 2D triangular antiferromagnet is investigated using the t-J model. The one-hole states are described by strings of spin deviations around the hole. Using projection technique the one-hole spectral function is calculated. For large J/t we find low-lying quasiparticle-like bands which are well separated from an incoherent background by a gap of order J. However, for small J/t this gap vanishes and the spectrum becomes broad over an energy range of several t. The results are compared with SCBA calculations and numerical data.Comment: 4 pages, 6 figs, to be publish in PR

Open Heterotic Strings

We classify potential cosmic strings according to the topological charge measurable outside the string core. We conjecture that in string theory it is this charge that governs the stability of long strings. This would imply that the SO(32) heterotic string can have endpoints, but not the E_8 x E_8 heterotic string. We give various arguments in support of this conclusion.Comment: 15 pages. v.2: typos, references correcte

Calabi-Yau Fourfolds with Flux and Supersymmetry Breaking

In Calabi-Yau fourfold compactifications of M-theory with flux, we investigate the possibility of partial supersymmetry breaking in the three-dimensional effective theory. To this end, we place the effective theory in the framework of general N=2 gauged supergravities, in the special case where only translational symmetries are gauged. This allows us to extract supersymmetry-breaking conditions, and interpret them as conditions on the 4-form flux and Calabi-Yau geometry. For N=2 unbroken supersymmetry in three dimensions we recover previously known results, and we find a new condition for breaking supersymmetry from N=2 to N=1, i.e. from four to two supercharges. An example of a Calabi-Yau hypersurface in a toric variety that satisfies this condition is provided.Comment: 26 page

Developing Antidote Controlled Antiplatelet Therapies By Targeting The Vwf ‐ Gp Ib‐Ix‐V Interaction

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/106054/1/jth02400.pd