Information report for Glyma.08G161300.1.p
Gene Details
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Functional Annotation
- Refseq: XP_003531470.1 — NAC domain-containing protein 76
- Refseq: XP_028246932.1 — NAC domain-containing protein 76-like
- Swissprot: Q9MA17 — SMB_ARATH; Protein SOMBRERO
- TrEMBL: A0A0B2QN82 — A0A0B2QN82_GLYSO; Protein SOMBRERO
- TrEMBL: I1KTT9 — I1KTT9_SOYBN; Uncharacterized protein
- STRING: GLYMA08G17140.1 — (Glycine max)
- GO:0003002 — Biological Process — regionalization
- GO:0006355 — Biological Process — regulation of transcription, DNA-templated
- GO:0009834 — Biological Process — plant-type secondary cell wall biogenesis
- GO:0010455 — Biological Process — positive regulation of cell fate commitment
- GO:0048829 — Biological Process — root cap development
- GO:0005634 — Cellular Component — nucleus
- GO:0003677 — Molecular Function — DNA binding
Family Introduction
- NAM, ATAF, and CUC (NAC) transcription factors comprise a large protein family. Proteins of this family contain a highly conserved N-terminal DNA-binding domain and a variable C-terminal domain (Xie et al. 2000; Duval et al. 2002; Ernst et al. 2004; Olsen et al. 2005). NAC was originally derived from the names of three proteins, no apical meristem (NAM), ATAF1-2, and CUC2 (cup-shaped cotyledon), that contain a similar DNA-binding domain (Souer et al. 1996; Aida et al. 1997). The early reported NAC transcription factors are implicated in various aspects of plant development. A few examples are NAM from Petunia (Souer et al. 1996) and CUC1-2 (Aida et al. 1997) from Arabidopsis which have roles in controlling the formation of boundary cells of the meristem; NAP (Sablowski and Meyerowitz 1998) from Arabidopsis which acts as a target gene of AP3/PI and functions in the transition between cell division and cell expansion in stamens and petals; and AtNAC1 which mediates auxin signaling to promote lateral root development (Xie et al. 2000). Recently, a few NAC transcription factors were reported to play an essential role in regulating senescence, cell division, and wood formation (Ishida et al. 2000; Takada et al. 2001; Vroemen et al. 2003; Weir et al. 2004; Kubo et al. 2005; Kim et al. 2006; Zhong et al. 2006; Demura and Fukuda 2007; Ko et al. 2007; Mitsuda et al. 2007; Zhong et al. 2007).
- NAM, ATAF, and CUC proteins were also found to participate in plant responses to pathogens, viral infections, and environmental stimuli (Xie et al. 1999; Ren et al. 2000; Collinge and Boller 2001; Kim et al. 2007). In Arabidopsis, three NAC genes, ANAC019, ANAC055, and ANAC072, were induced by drought, salinity, and/or low temperature (Tran et al. 2004), and the transgenic Arabidopsis plants overexpressing these genes showed improved stress tolerance compared to the wild type (Tran et al. 2004). Furthermore, proteins of these genes can bind to a ciselement containing CATGTG motif (Tran et al. 2004).
Literature and News
Sequences
CDS Sequence:
- >Glyma.08G161300.1.p|Glycine_max|NAC|Glyma.08G161300.1.p
ATGATGCCAGGCAATGGACAGTTAACAGTTCCTCCGGGCTTCAGGTTCCACCCTACTGATGAGGAGCTTCTCTACTATTACCTGAGGAAGAAAGTTTCTTATGAAGCCATTGATCTTGATGTCATAAGAGAAGTAGATCTCAACAAACTTGAGCCTTGGGACCTCAATGATAAGTGTAGGATTGGGTCAGGGCCTCAGAATGAGTGGTATTTCTTCAGCCACAAGGACAAGAAGTACCCAACAGGAACCAGAACAAACCGAGCAACTACAGCTGGGTTTTGGAAAGCAACTGGGAGGGACAAGGCCATATACCACACTAATTCCAAGAGGATTGGCATGAGGAAAACCCTAGTTTTCTACACTGGTCGTGCTCCTCATGGCCAAAAGACTGATTGGATCATGCATGAGTATCGCCTTGATGAAGATGATGCTGATATTCAAGAAGATGGGTGGGTGGTATGCAGGGTGTTCAAAAAGAAAAGCCAAAACCGAGGTTTCCAGCAAGAAATTGAAGAAGAAGAGCACTTAACCACCCATATGAGAGCAAGTGGTCATTGCCAGGTCCTAGAGCCAAAGCATCATCACATGCAACAAGGACTCTATGATCACTACAACTTCGATGGGACAATGCATCTCCCACAGTTGTTCAGTCAAGAATCAGCAGTTGCACCACCCACAAATTCTTCCTTGGCCTCATCTATGAATGCCATGGACATCCTTCAGTGCTCTCAAAACCTCCTGAGGCTCACAACCACTACTGGCTGTGGACTTAATCTCATGCAGCAGCAACAACAACAAGGAGAGAGGTTCAGTGGTGACTGGTCTTTCTTGGACAAGCTACTAGCATCACACCATGGCATGGATCAAAGCAAATGTAACCCTCCTACTCATCATCAAGGTGCAAGTGTGGGAACTTCAGCTCAGAAATTCCCATTTCATTACCTTGGCTGTGACACCACCCATGATATCATGAAATTTTCCAAGTAG
Protein Sequence:
- >Glyma.08G161300.1.p|Glycine_max|NAC|Glyma.08G161300.1.p
MMPGNGQLTVPPGFRFHPTDEELLYYYLRKKVSYEAIDLDVIREVDLNKLEPWDLNDKCRIGSGPQNEWYFFSHKDKKYPTGTRTNRATTAGFWKATGRDKAIYHTNSKRIGMRKTLVFYTGRAPHGQKTDWIMHEYRLDEDDADIQEDGWVVCRVFKKKSQNRGFQQEIEEEEHLTTHMRASGHCQVLEPKHHHMQQGLYDHYNFDGTMHLPQLFSQESAVAPPTNSSLASSMNAMDILQCSQNLLRLTTTTGCGLNLMQQQQQQGERFSGDWSFLDKLLASHHGMDQSKCNPPTHHQGASVGTSAQKFPFHYLGCDTTHDIMKFSK*