Overgrowth of Pollen Tubes in Embryo Sacs of Rhododendron Following Interspecific Pollinations

1986 ◽  
Vol 34 (4) ◽  
pp. 413 ◽  
Author(s):  
EG Williams ◽  
V Kaul ◽  
JL Rouse ◽  
BF Palser

Frequent overgrowths of pollen tubes within the embryo sac are characteristic of a number of interspecific crosses in the genus Rhododendron (Ericaceae). The combined techniques of sectioning, squashing and whole-ovule clearing have confirmed that in ovules showing this phenomenon the pollen tube fails to terminate growth and release sperms on entry into a synergid; instead it continues to grow beyond the synergid and egg cell, often filling the main body of the embryo sac with a coiled and distorted mass. Such ovules fail to develop further. The occurrence and possible causes of this error syndrome are discussed.

HortScience ◽  
1991 ◽  
Vol 26 (5) ◽  
pp. 585-586 ◽  
Author(s):  
Sierd Zijlstra ◽  
Coen Purimahua ◽  
Pim Lindhout

Crossing barriers between white- and purple-flowered species were examined. Four accessions of Capsicum annuum and three of C. pubescens were reciprocally crossed with one to four accessions of C. baccatum, C. cardenasii, C. chacoense, C. chinense, C. eximium, C. frutescens, C. galapagoense, and C. praetermissum. Capsicum chacoense is the only white-flowered species that inhibits C. annuum pollen tube growth but allows C. pubescens pollen tube penetration into the egg cell. Capsicum cardenasii and C. eximium exhibit similar crossabilities with C. annuum and C. pubescens: pollen tubes of C. cardenasii and of C. eximium can penetrate the egg cells of C. annuum but not vice versa, and pollen tubes of C. pubescens can penetrate the egg cells of C. cardenasii and of C. eximium but not vice versa.


1986 ◽  
Vol 64 (2) ◽  
pp. 282-291 ◽  
Author(s):  
V. Kaul ◽  
J. L. Rouse ◽  
E. G. Williams

Early events in the embryo sac of Rhododendron kawakamii and R. retusum have been studied after compatible self-pollinations and eight interspecific crosses, using sectioned ovaries, pistil squashes, and seed-set data. Ovules of Rhododendron kawakamii and R. retusum are anatropous, unitegmic, and tenuinucellate, with a typical eight-nucleate, seven-celled embryo sac. Fertilization normally occurs 4–5 days after pollination. The zygote lays down a callose wall but remains undivided during the first 13–15 days after pollination. The primary endosperm nucleus divides soon after fertilization, and development is cellular ab initio. Crosses of R. kawakamii (♂) with R. santapaui and R. retusum and crosses of R. retusum (♂) with R. kawakamii, R. santapaui, R. ovatum, and R. tashiroi showed apparently normal fertilization in a majority of ovules entered by pollen tubes. In crosses of R. kawakamii (♂) with R. quadrasianum and Kalmia latifolia entry of pollen tubes into ovules was delayed and frequently abnormal. Apart from compatible self-pollinations of R. kawakamii an R. retusum, only the cross of R. kawakamii (♂) with R. santapaui produced healthy seedlings. Of the remaining seven interspecific crosses only three showed significant embryo development in control pistils left to mature in situ. Similarities and differences in the breeding behaviour of R. kawakamii and R. retusum are discussed with reference to their taxonomic grouping within subsection Pseudovireya.


1973 ◽  
Vol 12 (2) ◽  
pp. 403-419 ◽  
Author(s):  
D. DE NETTANCOURT ◽  
M. DEVREUX ◽  
A. BOZZINI ◽  
M. CRESTI ◽  
E. PACINI ◽  
...  

The experimental results obtained show that the tip of the incompatible pollen tube bursts open after the outer-wall has considerably expanded in the intercellular spaces of the conducting tissue and the inner-wall has disappeared and numerous particles have accumulated in the tube cytoplasm. These particles, which measure approximately 0.2 µm in diameter and give a weak reaction to the test of Thiéry, differ in many respects from the vesicles normally present in compatible pollen tubes growing through the style; they appear to resemble, in some cases, the spheres which are discharged by the compatible pollen tubes after they have reached the embryo-sac. It is considered that these observations support the current belief that the tube wall is the site of action for the incompatibility proteins and suggest that self-incompatibility is not a passive process resulting from lack of growth stimulation but an active event which leads to the destruction of the incompatible pollen tubes. The degradation mechanism involved appears similar to the one which enables the compatible pollen tube to release its contents in the degenerated synergid and presents some analogies with the lytic process taking place in virus-infected cells. The general hypothesis is presented that the particles observed in the cytoplasm of self-incompatible pollen tubes consist of a mixture of incompatibility proteins and of basic constituents of the tube wall.


Development ◽  
2000 ◽  
Vol 127 (20) ◽  
pp. 4511-4518 ◽  
Author(s):  
K.K. Shimizu ◽  
K. Okada

Sexual reproduction in plants, unlike that of animals, requires the action of multicellular haploid gametophytes. The male gametophyte (pollen tube) is guided to a female gametophyte through diploid sporophytic cells in the pistil. While interactions between the pollen tube and diploid cells have been described, little is known about the intercellular recognition systems between the pollen tube and the female gametophyte. In particular, the mechanisms that enable only one pollen tube to interact with each female gametophyte, thereby preventing polysperm, are not understood. We isolated female gametophyte mutants named magatama (maa) from Arabidopsis thaliana by screening for siliques containing half the normal number of mature seeds. In maa1 and maa3 mutants, in which the development of the female gametophyte was delayed, pollen tube guidance was affected. Pollen tubes were directed to mutant female gametophytes, but they lost their way just before entering the micropyle and elongated in random directions. Moreover, the mutant female gametophytes attracted two pollen tubes at a high frequency. To explain the interaction between gametophytes, we propose a monogamy model in which a female gametophyte emits two attractants and prevents polyspermy. This prevention process by the female gametophyte could increase a plant's inclusive fitness by facilitating the fertilization of sibling female gametophytes. In addition, repulsion between pollen tubes might help prevent polyspermy. The reproductive isolations observed in interspecific crosses in Brassicaceae are also consistent with the monogamy model.


1982 ◽  
Vol 53 (1) ◽  
pp. 255-277
Author(s):  
ELIZABETH G. WILLIAMS ◽  
BRUCE R. KNOX ◽  
JOHN L. ROUSE

The cytology of compatible and interspecific incompatible pollinations has been followed in selected species of the genus Rhododendron (Ericaceae). Pollinated pistils were fixed, cleared, stained in decolourized aniline blue, and observed by epifluorescence microscopy. Ten different abnormalities of arrested pollen tube tips have been detected, including burst, tapered, swollen, coiled, spiralling, spiky and variable diameter syndromes. A series of five errors of callose deposition in incompatible tubes has also been defined. Six different regions in the pistil for expression of pollen tube arrest have been found, including the stigmatic exudate, the mucilage of the upper and lower style canal, the ovary loculus, the micropyle. There may also be abnormal behaviour after entry into the embryo sac. Both the site of pollen tube arrest within the pistil, and the error syndrome of tip growth and callose deposition anomalies, are characteristic of each interspecific cross. These results are discussed in relation to the genetic control of reproduction.


1972 ◽  
Vol 50 (11) ◽  
pp. 2117-2124 ◽  
Author(s):  
Veronica A. Martinson

In a comparative study of embryo development in intraspecific (U6 × K5/353) and interspecific (U6 × T33) crosses of Theobroma, the development of the embryo sac as described by previous authors was confirmed. Disintegration of synergids showed that the growth of the pollen through the style was slightly quicker in intraspecific than in interspecific crosses, but the number of embryo sacs which had received male nuclei 3 days after pollination was about the same. Although gametic fusion and endosperm formation in the intraspecific cross was in advance of those in interspecific cross, the major blockage in species hybridization occurred subsequent to fertilization, and in most instances, well after the proembryo stage. Abnormal cell division and cell differentiation were contributory factors to poor seed formation. Possible causes of the abnormality have been discussed.Autonomous enlargement and the binucleate appearance of the egg cells in the unpollinated flower suggested a tendency to parthenogenesis and diploidization of the egg cell, under special conditions. Although a large proportion of the cacao seeds observed in the species crosses are most probably intraspecific seedlings arising from contamination after controlled pollinations, the occurrence of a small number of true maternal seeds cannot be ruled out altogether.


Zygote ◽  
1993 ◽  
Vol 1 (2) ◽  
pp. 143-154 ◽  
Author(s):  
Bing-Quan Huang ◽  
Elisabeth S. Pierson ◽  
Scott D. Russell ◽  
Antonio Tiezzi ◽  
Mauro Cresti

The cytoskeletal organisation of the isolated embryo sac and egg cells of Plumbago zeylanica was examined before, during and after pollen tube penetration into the embryo sac to determine the potential involvement of microtubules and actin filaments in fertilisation. Material was singly and triply stained using Hoechst 33258 to localise DNA, fluorescein isothiocyanate (FITC)-labelled anti- α-tubulin to detect microtubules and rhodamine-phalloidin to visualise F-actin. Microtubules in the unfertilised egg cell are longitudinally aligned in the micropylar and mid-lateral areas, aggregating into bundles near the filiform apparatus. In the perinuclear cytoplasm of the egg cell, microtubules become more or less randomly aligned. F-actin bundles form a longitudinally aligned mesh in the chalazal cytoplasm of the egg cell. In the central cell, microtubules and F-actin are distributed along transvacuolar strands and are also evident in the perinuclear region and at the periphery of the cell. During pollen tube penetration, sparse microtubule bundles near the pathway of the pollen tube may form an apparent microtubular ‘conduit’ surrounding the male gametes at the delivery site. Actin aggregates become organised near the pathway of the pollen tube and at the delivery site of the sperm cells. Subsequently, actin aggregates form a ‘corona’ structure in the intercellular region between the egg and central cell where gametic fusion occurs. The corona may have a role in maintaining the close proximity of the egg and central cell and helping the two sperm cells move and bind to their target cells. The cytoskeleton may also be involved in causing the two nuclei of the egg and central cell to approach one another at the site of gametic fusion and transporting the two sperm nuclei into alignment with their respective female nucleus. The cytoskeleton is reorganised during early embryogenesis.


1982 ◽  
Vol 30 (6) ◽  
pp. 601 ◽  
Author(s):  
M Sedgley

Floral anatomy and pollen tube growth in the quandong were studied using light and scanning electron microscopy. The flowers had four perianth lobes and four stamens whose anthers dehisced by longitudinal slits. The pollen became caught in long unicellular hairs adjacent to the anthers. The central disc secreted nectar through raised stomata. The stigma papilla cells had a cuticle with a rough surface overlying thick PAS-positive walls. The half-inferior ovary normally contained two ovules. The embryo sac extended beyond the ovule at the micropylar end and into the placenta at the chalazal end. Half of the ovaries observed at both anthesis and 4 days following anthesis had no embryo sacs and the other half had one embryo sac. Occasional ovaries had two embryo sacs and some underdeveloped embryo sacs were observed that did not extend beyond the ovule or into the placenta. Pollen tubes had reached the ovary by 1 day following pollination and the stigma was receptive for 8 days following anthesis. Only half of the pistils had pollen tubes in the ovary. Unpollinated flowers had no pollen tube growth in the pistil.


2018 ◽  
Vol 19 (12) ◽  
pp. 3710 ◽  
Author(s):  
Shujuan Zhang ◽  
Chunbo Wang ◽  
Min Xie ◽  
Jinyu Liu ◽  
Zhe Kong ◽  
...  

The angiosperm pollen tube delivers two sperm cells into the embryo sac through a unique growth strategy, named tip growth, to accomplish fertilization. A great deal of experiments have demonstrated that actin bundles play a pivotal role in pollen tube tip growth. There are two distinct actin bundle populations in pollen tubes: the long, rather thick actin bundles in the shank and the short, highly dynamic bundles near the apex. With the development of imaging techniques over the last decade, great breakthroughs have been made in understanding the function of actin bundles in pollen tubes, especially short subapical actin bundles. Here, we tried to draw an overall picture of the architecture, functions and underlying regulation mechanism of actin bundles in plant pollen tubes.


2014 ◽  
Vol 50 (1-2) ◽  
pp. 191-193 ◽  
Author(s):  
H. J. Wilms

The micropylar parts of nucellus and embryo sac were studied in relation to pollen tube growth and its entrance into the embryo sac. The initially homogeneous walls of the cells of the conductive nucellar tissue disintegrate at the middle lamellae region. Pollen tubes pierce the nucellar cuticle and continue their growth into the nucellus intercellularly. Subsequently they can follow various pathways to reach the FA of the degenerated synergid. The penetration into this synergid, and the discharge of the tube contents are described and discussed.


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