Identification of alternate dwarfing gene sources to widely used Dee-Gee-Woo-Gen allele of sd1 gene by molecular and biochemical assays in rice (Oryza sativa L.)
Lakshminarayana Reddy Vemireddy
Ebrahimali Abubacker Siddiq*
Keywords: Dee-Gee-Woo-Gen, dwarfing gene, gibberellic acid assay, molecular marker, rice, sd1 gene.
After the success of IR8 and TN1, breeders depended heavily on these two rice cultivars for source of short stature led to the narrow genetic base to majority of present day rice varieties, as far as sd1 (semi-dwarf1) gene is concerned. In addition, analysis of genetic lineage of the majority of the cultivated rice varieties in tropical Asia reveals that sd1 from DGWG (Dee-Gee-Woo-Gen) is the major source of dwarfing gene. Such high amount of genetic homogeneity renders rice plants vulnerable to epidemic of diseases and insect pests. In the current study, we made an attempt to identify the alternate sources of DGWG allele of sd1 gene by characterizing 29 induced and 3 spontaneous dwarf accessions employing marker for DGWG allele of sd1 gene and exogenous application of gibberellic acid (GA3). When occurrence of DGWG allele of sd1 gene and GA3 response were analyzed together, existence of two kinds of dwarfs was noticed viz., dwarf accessions with DGWG allele and dwarf accessions without DGWG allele of sd1 allele exhibiting varying responses to GA3. As many as 22 of 32 dwarf accessions showed absence of DGWG allele of sd1 gene with varying response to GA3 could be used as excellent alternate sources for DGWG allele of sd1 gene. These dwarf accessions could be used for broadening the genetic base for the plant height and thereby minimize the risk of genetic vulnerability. Our strategy of combining molecular and biochemical assays can be efficiently used for identifying alternate dwarfing gene sources to the Green Revolution gene sd1.
Rice is the staple food for more than one half of the world’s population. Tropical Asia accounting for over 90% of production and consumption of rice has been growing tall statured lodging prone varieties of very low yields until the advent of the non lodging high yielding semi-dwarf varieties in sixties. The short statured varieties developed using Dee-Gee-Woo-Gen (DGWG), a dwarf of spontaneous origin, have enabled many countries in the region to achieve self-sufficiency in rice in a short span of 15 years (Sasaki et al. 2002; Spielmeyer et al. 2002). Initial attempts to study the genetics of semi-dwarfism using crosses of traditional talls with semi-dwarf varieties indicated that it was controlled by a single recessive gene designated as sd1 (Singh et al. 1979; Cho et al. 1994). The sd1 gene has been reported to reduce plant height by 25% through approximately proportional reductions in lengths of the top five internodes; with practically no effect on panicle length (Rutger, 1984). Later, three research groups have mapped sd1 gene independently to chromosome 1 and shown to encode a GA20oxidase (GA20ox) (Monna et al. 2002; Sasaki et al. 2002; Spielmeyer et al. 2002), an enzyme that catalyzes the conversion of GA53 to GA20 in gibberellic acid (GA) biosynthesis. Semi-dwarf rice cultivars possessing the sd1 allele from DGWG are characterized by a 383bp deletion in the GA20ox gene that introduces a stop codon resulting in a highly truncated and inactive enzyme. Thus the normal height of the semi-dwarf rice is restored by exogenous application of GA (Ellis and Spielmeyer, 2002; Sasaki et al. 2002; Spielmeyer et al. 2002).
The success of DGWG gene based varieties such as IR8 and Taichung (Native) 1 has made breeders allover to depend excessively on these two rice cultivars for source of short stature. With over 90% of the high yielding varieties in cultivation today having DGWG gene (Kikuchi and Ikehashi, 1984; Cho et al. 1994; Spielmeyer et al. 2002), the genetic base, as result is quite narrow, as far as sd1 gene is concerned. Apprehending that genetic homogeneity to that high extent might render a vital character like plant type genetically vulnerable to sudden outbreak of diseases and insect pests, many efforts have been made since last two or three decades for broadening the genetic base through identification and use of alternate sources of dwarfing gene (Reddy and Padma, 1976; Singh et al. 1979). Genetic analysis of a large number of dwarfs of spontaneous and induced origin has revealed occurrence of dwarfs non-allelic to sd1 appears to be rare. Past efforts to identify dwarfing gene sources alternate to sd1 gene by conventional allelic relationships failed to yield desired results on account of difficulties experienced in phenotyping the segregating population and hybrid sterility in cross between dwarfs of indica and japonica origin.
In rice, as many as 61 dwarfing genes designated as d1 to d61 have been identified (Cho et al. 1994; Ashikari and Matsuoka, 2002). Even though many different dwarf accessions of mutant and spontaneous origin have been tried as alternate sources for developing semi-dwarf varieties, none other than sd1 locus of DGWG source proved to be of practical value. Different alleles of this locus have been used by scientists of Asia and America (Asano et al. 2007). Several of the dwarf mutants accumulated over a period have been characterized at molecular level and their dwarfness has been a attributed to defective signal transduction molecules like heterotrimeric-G protein (Ueguchi-Tanaka et al. 2000), homeobox like OSH15 (Sato et al. 1999), brassinosteriods (Yamamuro et al. 2000) and various GA biosynthesis genes (Sasaki et al. 2002; Itoh et al. 2004). Realizing the importance of broadening the genetic base for plant height, the present study was initiated to identify alternative dwarfing gene source(s) among a collection of induced and spontaneous mutants using molecular markers linked to sd1 locus that can distinguish DGWG allele type from the other alleles and exogenous application of GA.
Details of 34 rice genotypes comprising 29 induced and 3 spontaneous dwarf accessions, and two DGWG based semidwarf cultivars viz., TN1 and IR8 and screened to identify alternate sources to sd1 are summarized in Table 1. One tall variety (Nipponbare) was included as a check for PCR amplification of sd1 allele.
DNA of the experimental material was isolated following the modified potassium acetate method (Dellaporta et al. 1983).
Based on the 383bp deletion in sd1 allele of DGWG, reported PCR primers were used for detection of sd1 allele (Ellis and Spielmeyer, 2002). Sd1- F: 5’- CAC GCA CGG GTT CTT CCA GGT G -3’. Sd1- R: 5’- AGG AGA ATA GGA GAT GGT TTA CC- 3’.
Amplification of DNA was performed in 10 mM Tris-HCl pH 9.0, 50 mM KCl, 1.5mM MgCl2, 0.2 mM dNTPs, 1 U of Taq DNA polymerase (Bangalore Genei, India) and 30 ng of DNA per 20-µl reaction using a GeneAmp PCR system 9700 (PE Applied Biosystems, USA). After initial denaturation for 5 min at 94ºC, 35 cycles at each cycle comprised 30 sec denaturation at 94ºC, 30 sec annealing at 55ºC, 90 sec extension at 72ºC with a final extension for 10 min at 72ºC. Amplified products were mixed with bromophenol blue (gel loading dye) and were electrophoresed on a 2% agarose gel using 1 x Tris Borate buffer pH 8.0. The gels were stained in ethidium bromide and were documented using Alpha Imager 1220 (Alpha Innotech, USA).
Seeds of the experimental material were surface sterilized with 0.2% HgCl2 solution for 30 min and then washed with water. They were placed in petri dishes lined with wet filter paper and then kept in dark at 30ºC for two days for germination. Elongation of shoot was quantified by microdrop method (Mitsunaga et al. 1994). Ten uniformly germinated seeds were placed on a 1% agar plate-five for gibberellic acid treatment and five as controls and allowed to grow at 25ºC under fluorescent light till emergence of second leaf sheath. After two days, 1 μl of a solution of GA3 (10mg/ml) in ethanol was applied to coleoptile of rice seedlings. Three days after this treatment, the length of the second-leaf sheath was measured and average of 5 plants was taken to calculate GA3 response (GAR) as under: GAR= (GA3 treatment/control)*100.
Rice plants were grown in the greenhouse at 30ºC (day) and 24ºC (night).
Number of internodes and length of each of the internodes were recorded for at least five plants. Plant height was measured by actual measurement (cm) from soil surface to tip of the tallest panicle (awns excluded) from at least five plants.
In the present study, phenotypic data of 32 dwarf accessions and two semi-dwarf varieties were collected.
Number of internodes ranged from 2 to 4. Unlike the typical semi-dwarf varieties (4), most of the dwarf accessions (20) included in the study has 3 internodes (Figure 3A and Supplementary Figure 1). Two dwarf accessions viz., C-74 and C-81 have two internodes whereas remaining all (10) having four internodes like semi-dwarf rice varieties. Length of the first (top most internode in the plant) internode was found to account for more than 60% of the plant height in the accessions WL200, C-74, 408D and 468D (genotypes with two internodes were not considered). Only in two genotypes viz., WL90 and C-70 length of the second internode was more than the first internode. Length of the third and fourth internodes was highly variable ranging from 3.4 to 25.6% and 2 to 10%, respectively (Figure 3A). Plant height of the 32 dwarf accessions ranged from 30 cm to 96 cm. The height of the genotypes with four and three internodes ranged from 42 cm to 89 cm and 30 cm to 96 cm respectively. The height of the genotypes with two internodes ranged from 33 cm and 44 cm (Figure 3B).
In the present study, 32 dwarf accessions have screened for presence of DGWG allele of sd1 gene and GA response (Table 1). The dwarf accessions exhibited both DGWG allele of sd1 gene and moderate response to GA treatment were considered to be allelic to sd1 gene from DGWG and those behaving otherwise as alternates to DGWG allele of sd1 gene.
Based on the presence of DGWG allele of sd1 gene (348bp PCR product), 10 dwarf accessions viz., WL80, C-67, C-69, C-81, Aijuri, WL158, BijorII, 408D, C-74, and Chlorina were identified to be allelic to DGWG allele of sd1 gene and the rest as non-DGWG allele type of sd1 gene (Figure 1).
To characterize the “null allele” in 21 accessions that did not give any PCR product at the sd1 locus, we have used seven rice microsatellites (www.gramene.org) in upstream and two in downstream region of the sd1 gene with an average distance between markers is approximately 125kb (Supplementary Table 1). Although all induced dwarf accessions are treated with same mutagen i.e, gamma rays we have noticed different lengths of the sequence deletion around the sd1 gene. Of 32 dwarf accessions, it is surprising to note that, as many as 18 dwarf accessions showed the expansion of the deletion around the sd1 gene ranging from 59.82kb to 783.11kb (including the sd1 gene region). In some dwarf accessions viz., WL190, C-68 and 409D, the deletion is restricted to sd1 gene only. In remaining dwarf accessions deletion is restricted to DGWG allele of sd1 gene (383bp deletion) except WL244 in which full length sd1 gene is present. Either length of the expansion or presence or absence of the DGWG allele of the sd1 not matching to the response of the GA treatment. For instance, C-59 and 469D the length of the deletion is 192.56kb but their response to GA treatment is low and medium respectively.
Based on relative response to exogenously applied GA 3 , the dwarf accessions were grouped into three categories viz., highly sensitive (>300%), moderately sensitive (180-300%) and less sensitive (<180%) and 4, 18 and 10 accessions showed high, medium and low sensitive to GA 3 treatment, respectively (Figure 2).
When the results relating to presence of DGWG allele of sd1 gene and GA 3 response were taken together as many as 27 accessions were found to contain dwarfing gene other than that of DGWG (Table 2). Only five accessions viz ., WL80, C-67, C-69, C-81 and Aijuri allelic to DGWG allele of sd1.
Apprehending the genetic vulnerability of the present day semi-dwarf rice cultivars on account of their having one and the same dwarfing gene (sd1) for plant height (Cho et al. 1994; Spielmeyer et al. 2002) and keeping in view the need for alternate dwarfing gene sources of still higher physiological efficiency, the present attempt was made to identify alternate sources to DGWG allele of sd1 by characterizing of 29 induced (gamma rays) and 3 spontaneous dwarf accessions at physiological and molecular levels. Molecular assay was done using precise marker available for identifying DGWG allele of sd1 gene while physiological assay by sensitiveness to exogenously applied GA3. Generally, rice varieties with DGWG allele of sd1 gene reportedly exhibit moderate response to exogenously applied GA3 (Kumar and Singh, 1984; Hedden, 2003). When specific amplification of sd1 allele and GA3 response were analyzed together, existence of two kinds of dwarfs were noticed viz., dwarfs having sd1 allele and those characterized by absence of sd1 allele but with varying responses to GA3. Presence of DGWG allele of sd1 allele in the genotypes irrespective of their GA3 response as observed in the present study suggest involvement of various other GA biosynthesis related gene(s) in determining plant height. Mapping analysis of four GA 20ox-like genes viz., OsGA20ox1, OsGA20ox2, OsGA20ox3 and OsGA20ox4 reveal them to be located on chromosomes 3, 1, 7 and 5 respectively and OsGA20ox2 is identical to the rice green revolution gene sd1 (Sakamoto et al. 2004). OsGA20ox1 encoding an isoform of gibberellin 20-oxidase has been found to regulate of plant stature in rice (Oikawa et al. 2004). Other than GA 20 oxidase genes, ent-kaurene oxidase (KO) has been found to be implicated in determining semi-dwarf nature of Tan-Ginbozu (d35) (Itoh et al. 2004) and involvement of GA 3 oxidase-2 which encoded by the dwarf gene (d18) was reported to cause dwarf nature.
Though these dwarf mutants could be defective at one or the other steps in the GA biosynthetic pathway, which could be rescued by the application of GA. However, dwarfness need not always as a result of deficiency of GA- like substances but of other factors. For instance, the d1 type dwarf was reported to be defective in α-subunit of the heterotrimeric G protein affects gibberellin signal transduction (Ashikari et al. 1999; Ueguchi-Tanaka et al. 2000). Likewise, loss of function mutation in the rice homeobox gene OSH15 was also reported to affect the architecture of internodes resulting in d6dwarf plants (Sato et al. 1999). Characterization of dwarfs of d61 mutants reveals a protein kinase with high similarity to a putative brassinosteroid receptor in Arabidopsis to be linked to prevention of internode elongation (Yamamuro et al. 2000). A brassinosteroid-deficient mutant, ebisu dwarf d2 has been reported to be caused by loss of function of a new member of cytochrome P450 (Hong et al. 2002).
Difference in plant height in general between tall and semidwarf types in particular is mainly due to differences in the length of the first (subtending panicle) and the second (subtending flag leaf/stem) internodes (Harada and Vergara, 1972). In the present study, internodal length has been found to vary with genotypes. Some genotypes like WL131, C-68, C-59, C-70 and Aijuri are characterized by the noticeably shortened lower internodes without significant reduction in the length of panicle. Such plant types among the dwarfs studied might be value as potential genetic resources for evolving non lodging ideotypes of high productivity. The pattern of internodal elongation is like that of sd1 but with twin advantages as of having their centre of gravity relatively at lower position thereby enabling the plant to withstand lodging and the long upper internode causing least reduction in panicle length and facilitating better panicle emergence. Though dwarf mutatnts of japonica could be classified based on the elongation pattern of upper four internodes into dn, dm, d6, sh and nl types (Takeda, 1977; Sato et al. 1999), the dwarf genotypes included in the present study could not be classified into such groups, as their tall parent of the genotypes (unknown for majority of them) are not included. However, the following two specific patterns were noted other than normal ratio, viz., (i) length of second internode exceeding that of the first internode in accessions like WL90, C-70 and (ii) Excessive shortening of internodes below the second internode in accessions like C-70.
Genetic dwarfing is generally associated with reduction of internode length or decrease in internode number or both (Futsuhara et al. 1967). The present finding based on a variety of dwarf accessions of both induced and spontaneous origin suggest that number of internodes was not as much associated as length of internodes with plant height.
Most of the dwarf mutants identified in rice are not used in crop improvement because they are associated with one or other undesirable traits like severe dwarfism, sterility, or abnormal plant height and grain development etc. Some of the dwarf mutants in the present study have been found to be of good phenotypes characterized by inhibition of elongation of lower internodes, least reduction of length of top two internodes and hence normal panicle size, erect foliage etc (Supplementary Figure 1). They could be useful profitably be exploited in breeding for alternate ideal plant types, if the severity of their dwarfism were controlled.
In summary, dwarfing appears to be caused by different mechanisms, as observed in the present study as well as from earlier reports (Huang et al. 1996; Sakamoto et al. 2003). The success of sd1 of DGWG was attributed to right combination of the defective OsGA20ox2 to reduce plant height and expression of other GA 20-oxidase (s) including OsGA20ox1 to balance normal development or reproduction related systems (Sasaki et al. 2002). Presence of sd1 allele in genotypes differing in their level of GA3 response such as WL158, BijorII, 408D, C-74 and Chlorina found in the present study suggest involvement of various other genes that are not included in the GA biosynthesis in determining the plant height. Although the dwarf accessions belonging to this group are allelic to sd1, they might be associated with modifier genes of different strengths in biosynthesis of GA. In addition, most of the accessions 22 of 32, showed absence of DGWG allele of sd1 gene with varying response to GA3. The dwarf accessions without sd1 gene but with responding variedly to GA treatment could be used as excellent alternate sources for sd1 gene tentatively designated as “asd1”. Even though one dwarf accession i.e, WL244 produces functional protein of OsGA20ox-2, its dwarfness appears to be controlled by genes which are not involved in pathway of GA biosynthesis. When amplification of the entire sd1 gene and its surrounding region tried, many dwarfs failed to give amplified PCR products indicating the 383bp deletion (DGWG allele) of sd1 gene is expanded downstream and upstream of the sd1 gene and this expansion of sequence deletion ranging from 59.82kb to 783.11kb. This clearly suggests that the sd1 locus is either highly mutable or it might have undergone high selection pressure since beginning of green revolution on account of the extensive continuous and excessive cultivation of sd1 gene based varieties since their advent in the mid sixties. Contrary to the generally held view, spontaneous dwarf mutants are largely allelic to sd1 of DGWG (Singh et al. 1979), in the present study, one of the spontaneous dwarf accessions i.e., Area old seed could be non-allelic to sd1. Although further experiments are required to study the mode of inheritance of the newly non-allelic dwarfing genes, our strategy of combining molecular and biochemical assays can be efficiently used for identifying new alternate dwarfing gene sources to the Green Revolution gene sd1. Use of identified new sources of semi-dwarfism along with DGWG gene in future breeding programme could help greatly broaden the genetic base for the plant height and thereby minimize the risk of genetic vulnerability.
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