Pollen

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N. Aono, S. Miyazaki, T. Nishiyama, M. Hasebe

(saori@nibb.ac.jp, tomoakin@kenroku.kanazawa-u.ac.jp, mhasebe@nibb.ac.jp)

Interactions between the sporophytic non-reproductive cells, tapetum cells, and the sporogenous cells are necessary for both pollen and spore development. Both S. moellendorffii and P. patens had putative orthologues of five A. thaliana genes involved in these interactions (Ma, 2005); SERK1 and SERK2, EMS1/EXS, SPL/NZZ, and TPD1.

Meiosis is essential for eukaryotic sexual reproduction. Seven meiosis-related genes in A. thaliana (Caryl et al., 2003), including MEI1, ASK1, ASK2, ATK1, SYN1, MRE11, and ATRAD50, were well conserved in all of the land plant lineages.

Each microspore undergoes two mitotic divisions to form a vegetative cell and two sperm cells. Putative orthologues of MOR1 and DUO1, which are required to complete these mitotic divisions, were found in all land plants.

Pollen wall deposition begins soon after meiosis in A. thaliana. Defects in the pollen wall reduce pollen viability and fertility. We found putative orthologues of five genes involved in pollen wall deposition in S. moellendorffii and P. patens, including CER1, DEX1, YRE/FLP1/WAX2, MS2, and NEF1.

Pollen germinates and elongates a pollen tube after fertilization in angiosperms. Putative orthologues of ACA9, KIP, NPG1, POK, SEC8, SETH1, and SETH2, all of which are necessary for proper pollen tube germination and elongation, were identified in S. moellendorffii and P. patens.


References

Caryl, A.P., Jones, G.H., and Franklin, F.C. (2003). Dissecting plant meiosis using Arabidopsis thaliana mutants. J. Exp. Bot. 54, 25-38.

Ma, H. (2005). Molecular genetic analyses of microsporogenesis and microgametogenesis in flowering plants. Annu. Rev. Plant Biol. 56, 393-434.

Table of gene numbers

Gene functions Gene Gene used as a query The number of putative orthologs
Arabidopsis thaliana Oryza sativa Selaginalla moellendorffii (a) Physcomitrella patens
pollen AGL30, AGL65, AGL66, AGL94, and AGL104 MIKC*-type MADS-box genes 5) 6 3 3 (6) 11
Pollen EMS1/EXS EMS1 1 2 2 (2) 6
Pollen SPL/NZZ SPL 1 1 2 (4) 3
Pollen TPD1 3) TPD1 4 14 5 (9) 9
Pollen GPAT1 2) GPAT1 8 15 10 (20) 7
Pollen MEI1 MEI1 1 1 1 (2) 1
Pollen CDC45 CDC45 1 2 1 (2) 1
Pollen ATK1 ATK1 4 3 2 (4) 2
Pollen TES/STD TES 2 1 1 (2) 3
Pollen MRE11 MRE11 1 1 1 (2) 1
Pollen ATRAD50 ATRAD50 1 1 1 (2) 1
Pollen MMD1/DUET 7) MMD1 4 2 1 (2) 2
Pollen MS5 3) MS5 5 4 2 (4) 7
Pollen SYN1 SYN1 1 1 1 (2) 1
Pollen NEF1 NEF1 1 1 1 (2) 1
Pollen AMS AMS 1 1 1 (2) 2
Pollen YRE/FLP1/WAX2 CER1 1 3 3 (6) 2
Pollen DEX1 DEX1 1 1 2 (4) 1
Pollen MS2 MS2 2 1 2 (4) 2
Pollen ADL1C ADL1C 3 3 3 (6) 5
Pollen DUO1 DUO1 1 1 2 (4) 2
Pollen BCP1 BCP1 6) 2 0 0 0
Pollen CER1 CER1 3 5 1 (2) 2
Pollen MYB4 and 32 MYB4 6 6 2 (4) 0
Pollen QRT3 QRT3 2 1 0 2
Pollen AT2G19620 AT2G19620 3 4 1 (2) 7
Pollen AT5G56200 2) AT5G56200 9 8 2 (3) 4
Pollen SEC8 SEC8 1 1 1 (2) 3
Pollen POK POK 2 1 1 (2) 1
Pollen NPG1 2) NPG1 3 3 2 (4) 2
Pollen ACA9 7) ACA9 6 4 2 (4) 3
Pollen ATAPY2 ATAPY2 2 8 1 (2) 3
Pollen KIP KIP 2 1 1 (2) 1
Pollen GCS1 GCS1 1 2 1 (2) 1

footnote: The number of putative orthologs here refers to number of genes that is included in a clade that corresponds to all genes derived from a single gene in the last common ancestor of P. patens, S. moellendrffii, A. thaliana, and O. sativa based on phylogenetic analyses. The alignments and trees are available through http://moss.nibb.ac.jp/treedb/ (a) number of putative loci at first and number of putative alleles detected in parentheses. That is, 1 (2), indicates we found two sequences that likely represent two alleles of one locus. See Methods for brief methods.

Table of gene models in the assembly

protein id gene name named by other model name by
EMS1a-1 Saori Miyazaki
60277 EMS1a-2
99902 EMS1b-1
103725 EMS1b-2 Saori Miyazaki
438336 SPL1-1
444448 SPL1-2
113463 TPD1A-1
129580 TPD1A-2
92327 TPD1B1-1
92521 TPD1B2-1
114201 TPD1B1-2
114397 TPD1B2-2
451574 TPD1C1-1
451575 TPD1C1-2
451573 TPD1C2-1
451576 TPD1C2-2
170163 GPAT1-1
184962 GPAT1-2
170164 GPAT2-1
269600 GPAT2-2
80614 GPAT3-1
102257 GPAT3-2
405228 GPAT4-1
415055 GPAT4-2
118155 GPAT5-1
235331 GPAT5-2
405007 GPAT6-1
414847 GPAT6-2
63752 GPAT7-1
130920 GPAT7-2
107343 GPAT8-1
110944 GPAT8-2
90219 GPAT9-1
130719 GPAT9-2
80075 GPAT10-1
102271 GPAT10-2
451419 MEI1-1
446235 MEI1-2
425073 CDC45-1
235830 CDC45-2
78149 ATK1A-1
78306 ATK1A-2
84710 ATK1B-1
95452 ATK1B-2
91165 ZWI-1
187058 ZWI-2
126650 TES-1
135047 TES-2
451577 MRE11-1
451578 MRE11-2
405818 RAD50-1
136622 RAD50-2
31177 MMD1-1
31178 MMD1-2
451579 MS5A-1
451580 MS5A-2
405259 MS5B-1
MS5B-2
451421 SYN1-1
415062 SYN1-2
92814 NEF1-1
121635 NEF1-2
451590 AMS-1
430203 AMS-2
99824 WAX2A-1
103982 WAX2A-2
164680 WAX2B-1
185167 WAX2B-2
437448 WAX2C-1
408343 WAX2C-2
230422 CER1-1
129942 CER1-2
50757 DEX1A-1
50714 DEX1A-2
451591 DEX1B
270198 MS2A-1
270623 MS2A-2
80322 MS2B-1
101717 MS2B-2
183216 DL1A-1
162617 DL1A-2
90013 DL1B-1
232702 DL1B-2
266589 DL1C-1
451592 DL1C-2
105848 SEC8-1
113161 SEC8-2
446594 POK-1
128449 POK-2
116971 DUO1A-1
118852 DUO1A-2
80215 DUO1B-1
39442 DUO1B-2
109587 MYB4A-1 450007 MYBX1 Tomas Matus
120788 MYB4A-2
39516 MYB4B-1
39507 MYB4B-2
39481 MYB4C-1
39454 MYB4C-2
439372 SF21-1
440255 SF21-2
450838 ZPT3A-1 Erik Vollbrecht
450836 ZPT3A-2 Erik Vollbrecht
451596 ZPT3B-1
451593 ZPT3B-2
451600 ACA9A-1
451372 ACA9A-2
118764 ACA9B-1
451597 ACA9B-2
233281 APY-1
183978 APY-2
146641 KIP-1
178845 KIP-2
451370 GCS1-1
451371 GCS1-2
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