Ibtip1 gene from sweet potato root and promoter thereof
A sweet potato and gene technology, applied in genetic engineering, plant gene improvement, peptide source, etc., can solve the unreported sweet potato TIP gene and other problems
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Embodiment 1
[0074] Replication of sweet potato IbTIP1 gene
[0075] The fibrous root tissue of sweet potato (Ipomoea batatas (L.) Lam.cv.White star) was dried for 6 hours and then isolated by CTAB method (Kim and Hamada, Biotechnol Lett 27, 1841-1845, 2005) RNA. mRNA was isolated using the Poly(A) Tract mRNA Isolation System (Promega), and a sweet potato dried-treated root cDNA library was prepared using the SMART cDNA library (library) construction kit (Clontech). The first titer of the library shows about 1.5×10 6 pfu / ml value. 983 kinds of EST clones were secured by analysis based on base sequences extracted at random.
[0076] The nucleotide sequence of the 5' portion of the cDNA was determined using T3 primers, and the information and data of related genes were confirmed by analyzing the Blast database of NCBI (www.ncbi.nlm.gov). Among them, by analyzing the data, the candidate gene that may show specific expression in dryness and roots was copied, that is, the TIP (tonoplast in...
Embodiment 2
[0078] The expression analysis of the IbTIP1 gene of each tissue of sweet potato
[0079]In order to analyze the expression state of each tissue of the sweet potato moisture transport channel protein gene IbTIP1 of the present invention isolated from the dried sweet potato root, RT-PCR was performed. Whole RNA was extracted from sweet potato tissues (leaves, stems, fibrous roots, thick roots, and storage roots) using the CTAB method (Kim and Hamada 2005), and then 2.5 μg of total RNA was used to synthesize cDNA using the ImPro-H Reverse Transcrirption System cDNA synthesis kit (Promega Corporation) Synthesize cDNA. The expression state of the IbTIP1 gene was investigated using IbTIP1 gene-specific primers and using Ex-Taq DNA polymerase (TaKaRa). Base sequences (Forward: 5'-GTCACGTAAACCCTGCTGTCAC-3': SEQ ID NO: 4) and (Reverse: 5'-GCTAGAATGTTGGCACCCACTA-3': SEQ ID NO: 5) were used as IbTIP1-specific primers.
[0080] As a result, the IbTIP1 gene was strongly expressed in fi...
Embodiment 3
[0082] Expression Analysis of the IbTIP1 Gene Based on Drying Treatment and Hormone Treatment
[0083] In order to analyze the degree of response of the IbTIP1 gene of the present invention according to the drying treatment, the leaves and fibrous root tissues of sweet potato were dried for different times (0, 1, 2, 4, 8, 16, 24 hours) and then used in the Examples The method in 2 was used to isolate RNA, and then synthesize cDNA separately. RT-PCR was performed using the AccelTaq Premix Kit (Gedocs) using the IbTIP1 gene-specific primers used in Example 2 above.
[0084] As a result, the IbTIP1 gene in the leaf tissue began to increase gradually after 1 hour after the drying process began, and showed an expression peak in 4-8 hours, and then showed a reduced state ( Figure 4a ). In contrast, no increase or decrease in the expression of IbTIP1 based on the drying treatment was observed in the fibrous root tissue. This may be due to the high expression level of IbTIP1 gene...
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