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Results: 5

1.
Figure 2

Figure 2. From: Expression pattern of a nuclear encoded mitochondrial arginine-ornithine translocator gene from Arabidopsis.

Functional complementation of yeast. The yeast strain Y02386 (arg11) was transformed with the empty vector pDR195 (A), or with AtmBAC2 cloned in pDR195 (B).

Elisabetta Catoni, et al. BMC Plant Biol. 2003;3:1-1.
2.
Figure 1

Figure 1. From: Expression pattern of a nuclear encoded mitochondrial arginine-ornithine translocator gene from Arabidopsis.

Structural model of AtmBAC2. The prediction was performed using the TMHMM program . Six hydrophobic domains are depicted as black boxes and the three mitochondrial energy transfer signatures as grey boxes (amino acid positions are given).

Elisabetta Catoni, et al. BMC Plant Biol. 2003;3:1-1.
3.
Figure 4

Figure 4. From: Expression pattern of a nuclear encoded mitochondrial arginine-ornithine translocator gene from Arabidopsis.

Expression of AtmBAC2 mRNA expression in different Arabidopsis organs (A) and in whole seedlings grown on different nitrogen sources (B). RNAs were extracted and converted to cDNA by reverse transcription, and a 267 bp AtmBAC2 fragment was amplified by 25 PCR cycles. As control, a 377 bp actin2 fragment was amplified simultaneously by 20 PCR cycles (ACT2).

Elisabetta Catoni, et al. BMC Plant Biol. 2003;3:1-1.
4.
Figure 5

Figure 5. From: Expression pattern of a nuclear encoded mitochondrial arginine-ornithine translocator gene from Arabidopsis.

GUS staining of Arabidopsis plants transformed with the AtmBAC2 promoter-GUS fusion. Histochemical analysis revealed promoter activity in 1, 2, 4, 7 and 21 days old plants (A to E). Details of expression in mature leaves (F and G); activity in inflorescences and flower (H and I), individual pollen grains (J) and siliques (K to M).

Elisabetta Catoni, et al. BMC Plant Biol. 2003;3:1-1.
5.
Figure 3

Figure 3. From: Expression pattern of a nuclear encoded mitochondrial arginine-ornithine translocator gene from Arabidopsis.

Phylogenetic analyses of AtmBAC2 and other mitochondrial carriers. The alignment was restricted to the conserved domains (between pos. 11 and 259 in AtmBAC2 amino acid sequence). Maximum parsimony analyses were performed using PAUP 4b10 with all amino acid characters unweighted and gaps scored as missing characters. Heuristic tree searches were executed using 1000 random sequence additions and the tree bisection-reconnection branch-swapping algorithm with random sequence analysis. The complete alignment was based on 342 sites; 306 were phylogenetically informative. At5g01340, NP195754; ScACR1, CAA80973; HsCT, NP005975; BtCT, P79110; ScCT, NP009850; At4g39460, NP568060; At1g34065, NP564436; At5g26200, NP197992; At1g72820, NP565048; At5g15640, NP568317; At1g14140, NP172866; At5g09470, NP196509; At2g22500, NP179836; At4g24570, NP194188; HsOGC, NP003553; AtDTC, CAC84549; StOMT, X99853; ScDIC, AAB71336; HsDIC, NP036272; HsUCP, NP003346; At3g54110, NP190979; At5g58970, NP568894; ScYpr021c, NP015346; CeGC, NP497274; DmGC, AAF57048; HsGC1, CAD21007; HsGC2, CAD21008; AtmBAC1, NP568670; AtmBAC2, NP178108; HsCarT, O43772; ScARG11, CAA60862; AnARG11, AAD44763; NcARG13, AAF87777.

Elisabetta Catoni, et al. BMC Plant Biol. 2003;3:1-1.

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