Skip to main content
Log in

Transcriptional state and distribution of poly(A) RNA and RNA polymerase II in differentiating Hyacinthus orientalis L. pollen grains

  • Original Article
  • Published:
Sexual Plant Reproduction Aims and scope Submit manuscript

Abstract

Spatial distribution of poly(A) RNA, hypophosphorylated Pol IIA, and hyperphosphorylated Pol IIO form of polymerase RNA II was characterized using immunofluorescence, immunogold and fluorescence in situ hybridization (FISH) techniques in relationship to transcriptional activity in the microspore and developing pollen of H. orientalis. During the course of pollen development our results reflected much higher transcriptional activity in the vegetative cell than in the generative cell. The highest levels of transcription in pollen cells were observed in young pollen grains, successively decreasing during pollen maturation, reaching a minimum just before anthesis. Levels of poly(A) RNA were higher in the vegetative cell than in the generative cell during all observed stages of pollen development. Accompanying physiological inhibition of the RNA synthesis in mature pollen cells was a strong accumulation of poly(A) RNA in the cytoplasm, especially in the vegetative cell. Alterations in transcriptional activity of differentiating pollen cells were accompanied by changes in the level and localization pattern of both forms of Pol II. During high transcriptional activity in the pollen nuclei, both forms of RNA Pol II occurred at the periphery of chromatin masses, as well as in the areas between them. A strong decrease in Pol IIO levels was observed in generative and vegetative nuclei as transcriptional activity of pollen cells apparently became inhibited. Finally, just before anthesis, an almost complete lack of the Pol IIO was observed in both pollen nuclei. In contrast, the level of Pol IIA significantly increased during the later stages of pollen development, in spite of apparent transcriptional inhibition in both pollen cells. This rich pool of the hypophosphorylated form of Pol II was located mainly over the central areas of condensed chromatin clumps, which was especially visible in the generative nucleus. Spatial and temporal aspects of RNA synthesis, including poly(A) RNA, as well as organization of transcriptional machinery appear to be closely related in developing pollen cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figs. 1–8
Figs. 9–12
Figs. 13–18
Figs. 19–25
Fig. 26

Similar content being viewed by others

References

  • Alves-Ferreira M, Wellmer F, Banhara A, Kumar V, Riechmann JL, Meyerowitz M (2007) Global expression profiling applied to the analysis of Arabidopsis stamen development. Plant Physiol 145:747–762

    Article  PubMed  CAS  Google Scholar 

  • Becker JD, Boavida LC, Carnerio J, Haury M, Feijó JA (2003) Transcriptional profiling of Arabidopsis tissues reveals the unique characteristics of the pollen transcriptome. Plant Physiol 133:713–725

    Article  PubMed  CAS  Google Scholar 

  • Bednarska E (1984) The differentiation of pollen cells in Hyacinthus orientalis L.—ultrastructural and metabolic studies. Post Biol Kom 11:585–587

    Google Scholar 

  • Bednarska E, Górska-Brylass A (1987) Ultrastructural transformations of nuclei in differentiating Hyacinthus orientalis L. pollen grain cells. Acta Soc Bot Pol 4:667–685

    Google Scholar 

  • Bentley DL (2005) Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors. Curr Opin Cell Biol 17:251–256

    Article  PubMed  CAS  Google Scholar 

  • Bregman DB, Du L, Van der Zee S, Warren SL (1995) Transcription-dependent redistribution of the large subunit of RNA polymerase II to discrete nuclear domains. J Cell Biol 129:287–298

    Article  PubMed  CAS  Google Scholar 

  • Colot HV, Rosbash M (1982) Behavior of individual maternal pA + RNA during embryogenesis of Xenopus laevis. Dev Biol 94:79–86

    Article  PubMed  CAS  Google Scholar 

  • Dirks RW, Snaar S (1999) Dynamics of RNA polymerase II localization during the cell cycle. Histochem Cell Biol 111:405–410

    Article  PubMed  CAS  Google Scholar 

  • Fakan S (1994) Perichromatin fibrils are in situ forms of nascent transcripts. Trends Cell Biol 4:86–90

    Article  PubMed  CAS  Google Scholar 

  • Grande MA, van der Kraan I, de Jong L, van Driel R (1997) Nuclear distribution of transcription factors in relation to sites of transcription and RNA polymerase II. J Cell Sci 110:1781–1791

    PubMed  CAS  Google Scholar 

  • Gray NK, Wickens MP (1998) Control of translation initiation in animals. Ann Rev Cell and Dev Biol 14:399–457

    Article  CAS  Google Scholar 

  • Honys D, Twell D (2003) Comparative analysis of the Arabidopsis pollen transcriptome. Plant Physiol 132:640–652

    Article  PubMed  CAS  Google Scholar 

  • Honys D, Twell D (2004) Transcriptome analysis of haploid male gametophyte development in Arabidopsis. Genome Biol 5:R85

    Article  PubMed  Google Scholar 

  • Juge F, Zaessinger S, Temme C, Wahle E, Simonelig M (2002) Control of poly(A) polymerase level is essential to cytoplasmic polyadenylation and early development in Drosophila. EMBO J 21:6603–6613

    Article  PubMed  CAS  Google Scholar 

  • Kornblihtt AR, de la Mata M, Fededa JP, Munoz MJ, Nogues G (2004) Multiple links between transcription and splicing. RNA 10:1489–1498

    Article  PubMed  CAS  Google Scholar 

  • Lee TI, Young RA (2000) Transcription of eukaryotic protein-coding genes. Annu Rev Genet 34:77–137

    Article  PubMed  CAS  Google Scholar 

  • Mascarenhas JP (1975) The biochemistry of angiosperm pollen development. Bot Rev 41:259–314

    Article  CAS  Google Scholar 

  • Mascarenhas JP (1990) Gene activity during pollen development. Annu Rev Plant Physiol 41:317–338

    Article  Google Scholar 

  • Mascarenhas JP (1993) Molecular mechanisms of pollen tube growth and differentiation. Plant Cell 5:1303–1314

    Article  PubMed  CAS  Google Scholar 

  • McCormick S (1993) Male gametophyte development. Plant Cell 5:1265–1275

    Article  PubMed  Google Scholar 

  • Pina C, Pinto F, Feijó JA, Becker JD (2005) Gene family analysis of the Arabidopsis pollen transcriptome reveals biological implications for cell growth, division control, and gene expression regulation. Plant Physiol 138:744–756

    Article  PubMed  CAS  Google Scholar 

  • Proudfoot N, O’Sullivan J (2002) Polyadenylation: a tail of two complexes. Curr Biol 12:R855–R857

    Article  PubMed  CAS  Google Scholar 

  • Raghavan V (1981) Distribution of poly(A)-containing RNA during normal pollen development and during induced pollen embryogenesis in Hyoscyamus niger. J Cell Biol 89:593–606

    Article  PubMed  CAS  Google Scholar 

  • Raghavan V (1989) mRNAs and a cloned histone gene are differentially expressed during anther and pollen development in rice (Oryza sativa L.). J Cell Sci 92:217–229

    PubMed  CAS  Google Scholar 

  • Reed R (2003) Coupling transcription, splicing and mRNA export. Curr Opin Cell Biol 15:326–331

    Article  PubMed  CAS  Google Scholar 

  • Sims RJ, Mandal SS, Reinberg D (2004) Recent highlights of RNA-polymerase-II-mediated transcription. Curr Opin Cell Biol 16:263–271

    Article  PubMed  CAS  Google Scholar 

  • Tupy J (1982) Alternation in polyadenylated RNA during pollen maturation and germination. Biol Plantarum 24:331–340

    Article  CAS  Google Scholar 

  • Tupy J, Süss J, Hrabetova E, Rihova L (1983) Developmental changes in gene expression during pollen differentiation and maturation in Nicotiana tabacum. Biol Plantarum 25:231–237

    Article  Google Scholar 

  • Willemse MTM, Van Went JL (1984) The female gametophyte. In: Johri BM (ed) Embryology of angiosperms. Springer, Berlin, pp 159–196

    Google Scholar 

  • Wilt FH (1977) The dynamics of maternal poly(A) containing mRNA in fertilized sea urchin eggs. Cell 11:673–681

    Article  PubMed  CAS  Google Scholar 

  • Xie SQ, Pombo A (2006) Distribution of different phosphorylated forms of RNA polymerase II in relation to Cajal and PML bodies in human cells: an ultrastructural study. Histochem Cell Biol 125:21–31

    Article  PubMed  CAS  Google Scholar 

  • Zeng C, Kim E, Warren S, Berget S (1997) Dynamic relocation of transcription and splicing factors dependent upon transcriptional activity. EMBO J 16:1401–1412

    Article  PubMed  CAS  Google Scholar 

  • Zienkiewicz K, Smolinski DJ, Bednarska E (2006) Distribution of poly(A) RNA and splicing machinery elements in mature Hyacinthus orientalis L. pollen grains and pollen tubes growing in vitro. Protoplasma 227:95–103

    Article  PubMed  CAS  Google Scholar 

  • Zienkiewicz K, Zienkiewicz A, Rodriguez-Garcia MI, Smolinski DJ, Swidzinski M, Bednarska E (2008) Transcriptional activity and distribution of splicing machinery elements during Hyacinthus orientalis pollen tube growth. Protoplasma 233:129–139

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgment

This work was supported by the grant of Polish Ministry of Science and Higher Education no. No.N303 290434.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Krzysztof Zienkiewicz.

Additional information

Communicated by Scott Russell.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary figures (PDF 2,568 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zienkiewicz, K., Zienkiewicz, A., Smoliński, D.J. et al. Transcriptional state and distribution of poly(A) RNA and RNA polymerase II in differentiating Hyacinthus orientalis L. pollen grains. Sex Plant Reprod 21, 233–245 (2008). https://doi.org/10.1007/s00497-008-0085-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00497-008-0085-9

Keywords

Navigation