ORYZA SATIVA MYOSIN XI B controls pollen development by photoperiod-sensitive protein localizations

Developmental Biology

Volumn 304, Issue 2, 2007, Pages 579-592

  Jiang, Shu Ye ^a   Cai, Minnie ^a   Ramachandran, Srinivasan ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

Myosin; Oryza sativa; Photoperiod; Pollen development; Untranslated region

Indexed keywords

HYBRID PROTEIN; MYOSIN; ORYZA SATIVA MYOSIN XIB; UNCLASSIFIED DRUG;

ANTHER; ARTICLE; ENVIRONMENTAL FACTOR; GENE INSERTION; GENE SEQUENCE; GENETIC ANALYSIS; MALE STERILITY; MUTANT; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOTOPERIODICITY; POLLEN; POLLEN DEVELOPMENT; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; RICE; TRANSCRIPTION INITIATION;

ORYZA SATIVA;

EID: 34047276448     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2007.01.008     Document Type: Article

References (54)

1. Ashley W.W.J.R., and Russell B. Tenotomy decreases reporter protein synthesis via the 3′-untranslated region of the β-myosin heavy chain mRNA. Am. J. Physiol., Cell Physiol. 279 (2000) C257-C265
2. Battelle B.A., Andrews A.W., Calman B.G., Sellers J.R., Greenberg R.M., and Smith W.C. A myosin III from Limulus eyes is a clock-regulated phosphoprotein. J. Neurosci. 18 (1998) 4548-4559
3. Berg J.S., Powell B.C., and Cheney R.E. A millennial myosin census. Mol. Biol. Cell 12 (2001) 780-794
4. Bezanilla M., Horton A.C., Sevener H.C., and Quatrano R.S. Phylogenetic analysis of new plant myosin sequences. J. Mol. Evol. 57 (2003) 229-239
5. Borrell A., Cutanda M.C., Lumbreras V., Goday J.A., Culianez-Maci F.A., and Pages M. Arabidopsis thaliana Atrab28: a nuclear targeted protein related to germination and toxic cation tolerance. Plant Mol. Biol. 50 (2002) 249-259
6. Clement C. Anther plastids in angiosperms. Bot. Rev. 67 (2001) 54-73
7. Clement C., and Audran J.C. Anther wall layers control pollen sugar nutrition in Lilium. Protoplasma 187 (1995) 172-181
8. Clement C., Chavant L., Burrus M., and Audran J.C. Anther starch variations in Lilium during pollen development. Sex. Plant Reprod. 7 (1994) 347-356
9. Curtis D., Lehmann R., and Zamore P.D. Translational regulation and development. Cell 81 (1995) 171-178
10. Frohman K.B., Dush M., and Marlin G. Rapid amplification of full-lengthcDNAs from rare transcripts: amplification using a single-specific oligonucleotide primers. Proc. Natl. Acad. Sci. U. S. A. 85 (1988) 8998-9002
11. Goldspink P., Sharp W., and Russell B. Localization of cardiac α-myosin heavy chain mRNA is regulated by its 39 untranslated region via mechanical activity and translational block. J. Cell Sci. 110 (1997) 2969-2978
12. Gu W., Deng Y.F., Zenklusen D., and Singer R.H. A new yeast PUF family protein, Puf6p, represses ASH1 mRNA translation and is required for its localization. Genes Dev. 18 (2004) 1452-1465
13. Hamada S., Sekimoto H., Tanabe Y., Tsuchikane Y., and Ito M. Isolation of myosin XI genes from the Closterium peracerosum-strigosum-littorale complex and analysis of their expression during sexual reproduction. J. Plant Res. 119 (2006) 105-113
14. Harms E., Kivimäe S., and Young M.W. Posttranscriptional and posttranslational regulation of clock genes. J. Biol. Rhythms 19 (2004) 361-373
15. Hashimoto K., Igarashi H., Mano S., Nishimura M., Shimmen T., and Yokota E. Peroxisomal localization of a myosin XI isoform in Arabidopsis thaliana. Plant Cell Physiol. 46 (2005) 782-789
16. Heslop-Harrison J., and Heslop-Harrison Y. Myosin associated with the surface of organelles, vegetative nuclei and generative cells in angiosperm pollen grains and tubes. J. Cell Sci. 94 (1989) 319-325
17. Hiei Y., Ohta S., Komari T., and Kumashiro T. Efficient transformation of rice (Oryza sativa L) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 6 (1994) 271-282
18. Holweg C., and Nick P. Arabidopsis myosin XI mutant is defective in organelle movement and polar auxin transport. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 10488-10493
19. Jefferson R.A. Assaying chimeric genes in plants: the GUS gene fusion system. Plant Mol. Biol. Rep. 5 (1987) 387-405
20. Jiang S.Y., and Ramachandran S. Identification and molecular characterization of myosin gene family in Oryza sativa genome. Plant Cell Physiol. 45 (2004) 590-599
21. Jiang S.Y., Chen Q.F., and Fang X.J. Identifying and mapping cDNA fragments related to rice photoperiod sensitive genic male sterility. Chin. Sci. Bull. 45 (2000) 536-540
22. Kinkema M., and Schiefelbein J. A myosin from a higher plant has structural similarities to class V myosins. J. Mol. Biol. 239 (1994) 591-597
23. Kolesnik T., Szeverenyi I., Bachmann D., Kumar C.S., Jiang S.Y., Ramamoorthy R., Cai M., Ma Z.G., Sundaresan V., and Ramachandran S. Establishing an efficient Ac/Ds tagging system in rice: large-scale analysis of Ds flanking sequences. Plant J. 37 (2004) 301-314
24. Kuersten S., and Goodwin E.B. The power of the 3′UTR: translational control and development. Nat. Rev., Genet. 4 (2003) 626-637
25. Li X., Lu Q., Wang F., Xu C., and Zhang Q. Separation of the two-locus inheritance of photoperiod sensitive genic male sterility in rice and precise mapping the pms3 locus. Euphytica 119 (2001) 343-348
26. Liu Y.G., and Whittier R.F. Thermal asymmetric interlaced PCR: automatable amplification and sequencing of insert end fragments from P1 and YAC clones for chromosome walking. Genomics 25 (1995) 674-681
27. Liu L., Zhou J., and Pesacreta T.C. Maize myosins: diversity, localization, and function. Cell Motil. Cytoskeleton 48 (2001) 130-148
28. Mazumder B., Seshadri V., and Fox P.L. Translational control by the 3′-UTR: the ends specify the means. Trends Biochem. Sci. 28 (2003) 91-98
29. Mei M.H., Dai X.K., Xu C.G., and Zhang Q. Mapping and genetic analysis of the genes for photoperiod-sensitive genic male sterility in rice using the original mutant Nongken 58S. Crop Sci. 39 (1999) 1711-1715
30. Mermall V., Post P.L., and Mooseker M.S. Unconventional myosins in cell movement, membrane traffic, and signal transduction. Science 279 (1998) 527-533
31. Mignone F., Grillo G., Licciulli F., Iacono M., Liuni S., Kersey P.J., Duarte J., Saccone C., and Pesole G. UTRdb and UTRsite: a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs. Nucleic Acids Res. 33 (2005) D141-D146
32. Miller D.D., Scordilis S.P., and Hepler P.K. Identification and localization of three classes of myosins in pollen tubes of Lilium longiflorum and Nicotiana alata. J. Cell Sci. 108 (1995) 2549-2563
33. Mittag M. Conserved circadian elements in phylogenetically diverse algae. Proc. Natl. Acad. Sci. U. S. A. 93 (1996) 14401-14404
34. Okazaki K., Kawada J., Kunishige M., and Murakami K. Introduction of the characteristics of lilium-concolor into L X Asiatic hybrids by crossing through style-cutting pollination and embryo culture. J. Jpn. Soc. Hortic. Sci. 63 (1995) 825-833
35. Park S.K., Howden R., and Twell D. The Arabidopsis thaliana gametophytic mutation gemini pollen1 disrupts microspore polarity, division asymmetry and pollen cell fate. Development 125 (1998) 3789-3799
36. Radford J.E., and White R.G. Localization of a myosin-like protein to plasmodesmata. Plant J. 14 (1998) 743-750
37. Ramachandran S., and Sundaresan V. Transposons as tools for functional genomics. Plant Physiol. Biochem. 39 (2001) 243-252
38. Reddy A.S.N., and Day I.S. Analysis of the myosins encoded in the recently completed Arabidopsis thaliana genome sequence. Genome Biol. 2 (2001) 1-17
39. Reichelt S., Knight A.E., Hodge T.P., Baluska F., Samaj J., Volkmann D., and Kendrick-Jones J. Characterization of the unconventional myosin VIII in plant cells and its localization at the postcytokinetic cell wall. Plant J. 19 (1999) 555-567
40. Scott L., LaFoe D., and Weil C.F. Adjacent sequences influence DNA repair accompanying transposon excision in maize. Genetics 142 (1996) 237-246
41. Shimmen T., Ridge R.W., Lambiris I., Plazinski J., Yokota E., and Williamson R.E. Plant myosins. Protoplasma 214 (2000) 1-10
42. Song Z.P., Lu B.R., and Chen J.K. A study of pollen viability and longevity in Oryza rufipogon, O. sativa, and their hybrids. Int. Rice Res. Newsl. 26 (2001) 31-32
43. Staiger C.J., Baluska F., Volkmann D., and Barlow P. Actin: A Dynamic Framework for Multiple Plant Cell Functions (2000), Kluwer Academic Publishers, Boston, USA
44. Tang X., Hepler P.K., and Scordilis S.P. Immunochemical and immunocytochemical identification of a myosin heavy chain polypeptide in Nicotiana pollen tubes. J. Cell Sci. 92 (1989) 569-574
45. Thompson J.D., Gibson T.J., Plewniak F., Jeanmougin F., and Higgins D.G. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 25 (1997) 4876-4882
46. Tominaga M., Kojima H., Yokota E., Orii H., Nakamori R., Katayama E., Anson M., Shimmen T., and Oiwa K. Higher plant myosin XI moves processively on actin with 35 nm steps at high velocity. EMBO J. 22 (2003) 1263-1272
47. Virmani S.S., Sun Z.X., Mou T.M., Jauhar Ali A., and Mao C.X. Two-Line Hybrid Rice Breeding Manual (2003), International Rice Research Institute, Los Banos, Philippines
48. Wang Z., and Pesacreta T.C. A subclass of myosin XI is associated with mitochondria, plastids, and the molecular chaperone subunit TCP-1α in maize. Cell Motil. Cytoskeleton 57 (2004) 218-232
49. Wang S.H., Chen F., and Zhou K.D. In vitro pollen germination of rice. Acta Agron. Sin. 26 (2000) 609-612 (in Chinese)
50. Yamashita R.A., Sellers J.R., and Anderson J.B. Identification and analysis of the myosin superfamily in Drosophila: a database approach. J. Muscle Res. Cell Motil. 21 (2000) 491-505
51. Yang W.C., Ye D., Xu J., and Sundaresan V. The SPOROCYTELESS gene of Arabidopsis is required for initiation of sporogenesis and encodes a novel nuclear protein. Genes Dev. 13 (1999) 2108-2117
52. Yokota E., Yukawa C., Muto S., Sonobe S., and Shimmen T. Biochemical and immunocytochemical characterization of two types of myosins in cultured tobacco bright yellow-2 cells. Plant Physiol. 121 (1999) 525-534
53. Zhang Q., Shen B.Z., Dai X.K., Mei M.H., Saghai Maroof M.A., and Li Z.B. Using bulked extremes and recessive class to map genes for photoperiod-sensitive genic male sterility in rice. Proc. Natl. Acad. Sci. U. S. A. 91 (1994) 8675-8679
54. Zhang B., Gallegos M., Puoti A., Durkin E., Fields S., Kimble J., and Wickens M.P. A conserved RNA-binding protein that regulates sexual fates in the C. elegans hermaphrodite germ line. Nature 390 (1997) 477-484