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7 publications mentioning ath-MIR400

Open access articles that are associated with the species Arabidopsis thaliana and mention the gene name MIR400. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary.

1
[+] score: 17
These are two of the five miRNAs showing a transient increased expression during germination before decreasing in abundance at the end of the time course For other miRNAs, such as miR781a and miR400, their target genes are known [64] and these are differentially regulated during seed germination (Fig.   6c(i), (ii)). [score:6]
These are two of the five miRNAs showing a transient increased expression during germination before decreasing in abundance at the end of the time course For other miRNAs, such as miR781a and miR400, their target genes are known [64] and these are differentially regulated during seed germination (Fig.   6c(i), (ii)). [score:6]
c Expression profiles of (i) miRNA781a and (ii) miRNA400 (and their target genes), which are known for a role in other (non-germination) conditions/stages in Arabidopsis. [score:5]
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2
[+] score: 16
The miR400 was down-regulated, whereas its targets, PPR1 and PPR2, were up-regulated when the plants were challenged with pathogenic bacteria or fungi 52. [score:9]
On the contrary, miR156, miR158, miR164, miR165, miR400, miR5654, miR775, miR829, miR838 and miR852 were down-regulated by TCV infection. [score:4]
In our results, three TCV responsive miRNAs (miR158, miR400 and miR5654) which target PPR genes were decreased after TCV infection. [score:3]
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3
[+] score: 11
Such heat stress -induced alternative splicing also regulates the miR400 expression in Arabidopsis (Yan et al., 2012). [score:4]
This alternative splicing event may be favorable for thermotolerance, as overexpression of MIR400 made the plants more sensitive to heat stress (Yan et al., 2012). [score:3]
Upon heat stress, a specific alternative splicing occurred at the first intron of At1g32583 containing the miR400 hairpin, which led to a decrease of mature miR400, but did not affect the host gene expression. [score:3]
The intronic MIR400 is co-transcribed with its host gene At1g32583. [score:1]
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4
[+] score: 10
Another non-conserved miRNA, miR173, targets tasiRNA primary transcripts (TAS1 and TAS2) [34], which in turn yield siRNAs that also target several of the miR161- and miR400 -targeted PPR transcripts ([29]; data not shown). [score:7]
Interestingly, several non-conserved miRNAs (miR161 and miR400) target transcripts from a clade within the large PPR family [19], [41]. [score:3]
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5
[+] score: 7
In other studies, Arabidopsis plants overexpressing either miR400 or miR844 showed much severe disease symptoms compared to wild-type plants when challenged with pathogenic bacteria (P. syringae pv tomato DC3000) or fungi (Botrytis cinerea) (Park et al. 2014; Lee et al. 2015). [score:4]
MiR400 guides the cleavage of transcripts encoding pentatricopeptide repeat (PPR) proteins, whereas miR844 targets cytidinephosphate diacylglycerol synthase3 (CDS3) transcripts. [score:3]
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6
[+] score: 4
Other miRNAs from this paper: ath-MIR156a, ath-MIR156b, ath-MIR156c, ath-MIR156d, ath-MIR156e, ath-MIR156f, ath-MIR157d, ath-MIR158a, ath-MIR159a, ath-MIR160a, ath-MIR160b, ath-MIR160c, ath-MIR161, ath-MIR162a, ath-MIR162b, ath-MIR163, ath-MIR164a, ath-MIR164b, ath-MIR165a, ath-MIR165b, ath-MIR166a, ath-MIR166b, ath-MIR166c, ath-MIR166d, ath-MIR166e, ath-MIR166f, ath-MIR166g, ath-MIR167a, ath-MIR167b, ath-MIR169a, ath-MIR170, ath-MIR172a, ath-MIR172b, ath-MIR173, ath-MIR159b, ath-MIR319a, ath-MIR319b, ath-MIR167d, ath-MIR169b, ath-MIR169c, ath-MIR169d, ath-MIR169e, ath-MIR169f, ath-MIR169g, ath-MIR169h, ath-MIR169i, ath-MIR169j, ath-MIR169k, ath-MIR169l, ath-MIR169m, ath-MIR169n, ath-MIR171b, ath-MIR172c, ath-MIR172d, ath-MIR391, ath-MIR395a, ath-MIR395b, ath-MIR395c, ath-MIR395d, ath-MIR395e, ath-MIR395f, ath-MIR397a, ath-MIR397b, ath-MIR398a, ath-MIR398b, ath-MIR398c, ath-MIR399a, ath-MIR399b, ath-MIR399c, ath-MIR399d, ath-MIR399e, ath-MIR399f, ath-MIR408, ath-MIR156g, ath-MIR156h, ath-MIR158b, ath-MIR159c, ath-MIR319c, ath-MIR164c, ath-MIR167c, ath-MIR172e, ath-MIR447a, ath-MIR447b, ath-MIR447c, ath-MIR773a, ath-MIR775, ath-MIR822, ath-MIR823, ath-MIR826a, ath-MIR827, ath-MIR829, ath-MIR833a, ath-MIR837, ath-MIR841a, ath-MIR842, ath-MIR843, ath-MIR845a, ath-MIR848, ath-MIR852, ath-MIR824, ath-MIR854a, ath-MIR854b, ath-MIR854c, ath-MIR854d, ath-MIR857, ath-MIR864, ath-MIR2111a, ath-MIR2111b, ath-MIR773b, ath-MIR841b, ath-MIR854e, ath-MIR833b, ath-MIR156i, ath-MIR156j, ath-MIR826b
Under –N conditions, miR165, miR167c, miR171b/c, miR172c–e, miR773, miR823, miR824, miR826, miR829.1, and miR842 were induced specifically, whereas miR157d, miR158a, miR161.2, miR400, miR447, miR822, miR833-5p, miR843, and miR852 were suppressed. [score:3]
For example, miR163, miR773, miR843, miR848, and miR854-3p were responsive to –C; miR158a, miR161.2, miR400, miR447, miR773, miR822, miR823, miR826, miR833-5p, miR843, and miR852 were responsive to –N; and miR845a was responsive to –S. [score:1]
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7
[+] score: 1
In Arabidopsis, heat stress -induced AS of the precursor of miR400 resulted in the accumulation of primary transcripts and reduced levels of mature transcripts (Yan et al., 2012). [score:1]
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