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1.
A set of 21 monosomic (2n ‐ 1) and the disomic (2n) lines of the ‘Chinese Spring’ cultivar were crossed with ‘Chirya‐3′, the CIMMYT synthetic wheat line which has been identified as highly resistant for Helminthosporium leaf blight disease (HLB), in order to locate the genes governing disease resistance. The F1 and segregating populations were challenged and screened against the most virulent pure mono‐conidial HLB isolate KL‐8 (Karnal, India). The F1 progenies of the crosses were found to be susceptible because of the recessive nature of resistance. The F2 progeny of the control cross (‘Chinese Spring’בChirya‐3’), segregated in the ratio of 1: 15 (resistant: susceptible), indicating that resistance to HLB was controlled by a pair of recessive genes. While the F2 progeny of 19 monosomic crosses segregated in the ratio of 1: 15 (resistant: susceptible), the progeny of the remaining two crosses, 7B and 7D, deviated significantly from the ratio, revealing that 7B and 7D were the critical chromosomes for resistance genes that were located one on each chromosome. Moreover, the critical lines, 7B and 7D, confirmed the digenic complementary recessive nature of gene action by fitting well with the overall pooled F2 segregation ratio of 13: 51 (resistant: susceptible) as expected for digenic complementary recessive resistance. The F3 segregation ratios of the critical crosses, based on their pooled F2 analysis, was estimated as 19: 32: 13 (non‐segregating susceptible: segregating as susceptible and resistant: non‐segregating resistant). F3 progenies when tested with these ratios showed goodness‐of‐fit, confirming that the two pairs of recessive resistance genes were located on chromosomes 7B and 7D. 相似文献
2.
The homoeologous groups of chromosomes carrying the genes for some morphological traits in wild wheat Triticum turgidum L. ssp. dicoccoides (T. dicoccoides) were determined, but not the actual chromosomes carrying them. The objectives of this study were to investigate the modes
of inheritance, and determine the chromosomes carrying some morphological traits in wild emmer (2n = 28; AABB), the progenitor of most cultivated wheats. To investigate the inheritance of morphological traits, crosses were
made between T. turgidum L. ssp. durum (T. durum cultivar Chartokhmi (IR10) and T. dicoccoides accessions TA1150 and TA1131. F2 seeds from each cross were grown in the field and six qualitative characters were investigated. Purple coleoptile, purple
auricle, purple culm, hairy auricle, hairy rachilla, and fragility of spike were controlled by single dominant genes. To determine
the chromosomal locations, accession TA1131 was crossed with the complete set of LDN D-genome disomic substitution lines.
Assessments of F2 populations showed that chromosomes 7A, 6A, 7B, 5B, 5A and 3B carried genes for purple coleoptile, purple auricle, purple
culm, hairy auricle, hairy rachilla and brittle rachis, respectively. 相似文献
3.
The genes Ms2 for male sterility and Rht10 for dominant dwarfing located on the short arm of chromosome 4D in common wheat arc closely linked. Male sterile, dwarf F1 plants from the cross of male sterile‘Chinese Spring’× dwarf‘Ai-bian’were backcrossed with the variety‘Chinese Spring, From this offspring a spontaneous chromosome translocation was isolated resulting in a recombinant male sterile and dwarf genotype. 相似文献
4.
Detection of chromosomes carrying genes for seed dormancy of wheat using the backcross reciprocal monosomic method 总被引：6，自引：0，他引：6
Preharvest sprouting (PHS) in wheat represents a major constraint to the production of high‐quality grain. Genetic variation for tolerance to PHS is associated with seed dormancy. The present study was initiated to detect homologous chromosome variation associated with seed dormancy genes in a PHS tolerant cultivar ‘Zenkojikomugi’ (Zen) and ‘Chinese Spring’ (CS) using the backcross reciprocal monosomic method. The most striking effect on variation in seed dormancy was associated with chromosome 3A, and followed by group 4 chromosomes. These chromosomes of Zen increased dormancy compared with the respective CS homologues. Chromosomes 2D and 7D of Zen, and 6A of CS seemed to contribute smaller positive effects on dormancy. Chromosomes 2A of CS and Zen, as well as 3B, were equally effective in enhancing dormancy. The chromosome 3 A factors were independent of the grain‐colour gene R‐A1 because Zen was found to carry the white‐grained R‐A1a allele, which was identical to that of CS, and there was no difference in dormancy between the reciprocal F1 seeds. 相似文献
5.
干旱胁迫对小麦叶片细胞膜透性效应的染色体定位研究 总被引：5，自引：0，他引：5
通过测定干旱胁迫下小麦中国春-Synthetic 6x染色体代换系及其亲本品种中国春(受体)和Synthetic 6x(供体)叶片的相对电导率和K 相对渗出率,对调控干旱胁迫下功能叶片细胞膜稳定性的染色体进行了定位研究。结果表明,1D,2D,2B,3A,3D,4A,4B,6A,6B,7D和7A等染色体代换系的相对电导率和K 相对渗出率均显著或极显著低于中国春,而其他代换系差异均不显著。表明Synthetic 6x的1D,2B,2D,3A,3D,4A,4B,6A,6B,7D和7A染色体上具有耐旱性基因,而其他染色体与Synthetic 6x的耐旱性无关。研究结果可为小麦抗旱遗传育种研究提供参考依据。 相似文献
6.
干旱胁迫对小麦染色体代换系旗叶相对含水量和离体失水速率的影响 总被引：4，自引：0，他引：4
以中国春-Synthetic 6x小麦染色体代换系及其亲本为材料,对其旗叶相对含水量(RWC)、离体叶片失水速率(RWL)进行测定。结果表明,在干旱胁迫下,1A,2D和3D代换系叶片的相对含水量及其干旱/对照值显著或极显著高于中国春,3A,3B,4B,5B,6B,1D,2D和4D代换系叶片离体失水速率及其干旱/对照值显著或极显著低于中国春。由此表明,Synthetic 6x的1A,2D和3D染色体上可能存在干旱胁迫下调控相对含水量的基因,Synthetic 6x的3A,3B,4B,5B,6B,1D,2D和4D染色体上可能存在干旱胁迫下调控离体失水速率的基因。 相似文献
7.
Summary Several near-isogenic lines of durum wheat cv. LD222 have been developed. These include a near-isogenic line carrying gene P and designated P-LD222. The P gene from Triticum polonicum determines a long empty outer glume. The objective of this study was to determine the inheritance and chromosomal location of the P gene. To determine the inheritance, P-LD222 was crossed to two chlorina mutants and to a near-isogenic line for the purple culm trait, Pc-LD222. Linkage of the P gene with the mutated gene in chlorina mutant CDd6 indicated that the P gene was located on chromosome 7A. P-LD222 was also crossed with durum cultivar Langdon (LDN) and the LDN D genome substitution lines, LDN 7D(7A) and LDN 7D(7B). Segregation for the long glume trait in the F2 of LDN/P-LD222 and LDN 7D(7B)/P-LD222 was normal (3:1) and indicated P gene was not on chromosome 7B. Significant deviation from a 3:1 in the F2 of LDN 7D(7A)/P-LD222 confirmed the location of P on chromosome 7A, as indicated by the linkage analysis. 相似文献
8.
Six ‘Chinese Spring/Triticum spelta’ substitution lines for chromosomes 1A, 1D (duplicates), 3D (duplicates), 6D, and one ‘Chinese Spring/ Marquis’ substitution line for chromosome 2B were studied for tissue-culture response (TCR). The results reported here indicate that chromosomes 2B and 6D are critical for TCR, whereas chromosome ID affects callus weight only. Chromosomes 1A and 3D were not found to be critical, however, these chromosomes may carry genes with minor effects. 相似文献
9.
Summary Grain size in wheat is the most stable yield component and has a favorable effect on flour yield. To identify the chromosomes associated with the large grains of line G603-86, (grain weight over 60 mg and grain length of about 9 mm), F3 lines, extracted from F2 populations obtained from F1 monosomics of crosses between G603-86 (P1) and the monosomic set of Favorit (P2) were tested in the field. ANOVA showed significant differences among parents for grain weight and grain length, but not for grain width or the factor expressing the difference in grain form and density. Homoeologous groups had significant effects on grain weight and on all components of grain weight, while genomes were not significantly different for any of these characters. Grain weight was significantly increased by chromosomes 6D and 4A of G603-86. Grain length was significantly increased by chromosomes 4A, 4B, 2B, 3A and 1B, grain width by chromosomes 1A and 1B, and the factor form-density by chromosomes 6D and 6A. The high grain size in G603-86 results from the effects of genes located on many chromosomes which affect grain dimensions, form and density. 相似文献
10.
Summary F2 monosomic analysis and the direct comparisons between aneuploid series from different varieties of wheat suggest the likelihood of allelic variation. It is impossible however, from these studies to prove unequivocally that allelic variation exists. Some effects can be due to chromosome dosage rather than allelic variation. This disadvantage was overcome by using reciprocal monosomic analysis to study the genetic control of frost resistance on chromosome 5A in wheat. Data support the previous results obtained by F2 monosomic and substitution analysis. The chromosome 5A has been shown to be the one which carries the major allelic differences that distinguish wheat varieties Chinese Spring, Rannyaya 12 and Mironovskaya 808 for frost resistance. 相似文献
11.
Comparison of two fertility restoration systems against photoperiod-sensitive cytoplasmic male sterility in wheat 总被引：2，自引：0，他引：2
K. Murai 《Plant Breeding》2002,121(4):363-365
A ‘two‐line system’ using photoperiod‐sensitive cytoplasmic male sterility (PCMS) caused by Aegilops crassa cytoplasm under a long‐day photoperiod ( 15 h) has been proposed as a new means of producing hybrid varieties in common wheat. The PCMS line is maintained by self‐pollination under short‐day conditions, and hybrid seeds can be produced through outcrossing of the PCMS line with a pollinator under long‐day conditions. Two kinds of fertility restoration systems against the PCMS are known. One is involved with a set of multiple fertility‐restoring (Rf) genes in the wheat cultivar ‘Norin 61’ located on (at least) chromosomes 4A, 1D, 3D and 5D. The other is controlled by a single dominant major Rf gene, Rfd1, located on the long arm of chromosome 7B in the wheat cultivar ‘Chinese Spring’. To examine the degree of fertility restoration by these two systems, nine PCMS lines were crossed with ‘Norin 61’ and ‘Chinese Spring’ as the restorer lines, and the F1 hybrids were investigated. The degree of fertility restoration was estimated by comparing the seed set rates in the F1 hybrids having the Ae. crassa cytoplasm and those with normal cytoplasm. The results revealed that the fertility restoration ability of a set of multiple Rf genes in ‘Norin 61’ was higher than that of the Rfd1 gene in ‘Chinese Spring’. 相似文献
12.
Summary An Indian hexaploid wheat var. Pb C591 has been shown to carry gene(s) for chlorophyll synthesis on chromosome 3A (Singh & Joshi, 1979). In the present study cv. Pb.C591, its monosomic 3A and diteocentrics for 3A, 3BL and 3DL of var. Chinese Spring have been used. The F2 segregation involving crosses between Pb.C591 as male, monosomic line 3A of Pb.C591 (female) and ditelocentrics 3A, 3BL and 3DL of cv. Chinese Spring as male and female respectively has been observed. It has been found that there are two dominant genes regulating chlorophyll synthesis in cv. Chinese Spring. These genes are located on chromosomes arms 3A and 3DS respectively.These chlorophyll synthetic genes must be the same which were postulated by Sears (1956, 1957) as the normal alleles of virescent gene v
2 (which was located on 3BS) on chromosomes 3A(v
1) and 3D(V
3). 相似文献
13.
Chromosomal location of dwarfing gene Rht12 in wheat 总被引：2，自引：0，他引：2
Summary The chromosomal location of the dwarfing gene Rht12 in the mutant winter wheat Karcagi 522M7K was investigated using F2 monosomic analysis. The segregation ratio for F2 progenies of Chinese Spring monosomics × Karcagi 522M7K, and that of Cheyenne monosomics × Karcagi 522M7K indicated that the near complete dominant dwarfing gene Rht12 is located on chromosome 5A. The heterozygous and hemizygous states of the genes Rht12 have the same effect on plant height. 相似文献
14.
15.
The supernumerary spikelet (SS) character of bread wheat (Triticum aestivum L.) is an abnormal spike morphology expressing
extra spikelets per spike. Chromosomal location of the genes for the SS character in the bread wheat line, Yupi Branching
was determined by monosomic analysis. The normal-spiked bread wheat Chinese Spring monosomic series were used as testing lines.
Data indicated that chromosomes 2D, 4A, 4B and 5A of bread wheat carry genes for SS character (bh genes). Among them, the
gene on chromosome 2D has the strongest effect on the expression of the SS character. Comparison of disomic and monosomic
plants in 2D, 4A, 4B and 5A F2 populations revealed that the bh genes are hemizygous-effective and dosage-independent. The F1 monosomic analysis showed that the bh genes of Yupi Branching are recessive.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
16.
End-use quality of wheat for noodles is influenced by polyphenol oxidase activity and its corresponding substrates. This study investigated the chromosomal location of genes that determine phenol colour reaction of kernels in tetraploid wheat using aneuploid stocks. Polyphenol oxidase activity was estimated by the colour reaction of kernels to phenol solution. It was found that the genes located on homoeologous group 2 chromosomes have an important effect on the level of phenol colour reaction of kernels. The genes (Tc1 and Tc2) responsible for high phenol colour reaction of kernels were mapped to the long arms of chromosome 2A and chromosome 2B, respectively. The map distances were estimated to be 46.8 cM for Tc1 and 40.7 cM for Tc2 from the centromere using double-diltelosomics of durum wheat. 相似文献
17.
Summary Studies were made of days to ear emergence under the constant temperatures of 9, 14, 19 and 25°C and 16 h photoperiod in three sets of wheat lines each possessing genotypes differing for developmental responses.Days to ear emergence in three near-isogenic lines of the wheat cultivar Triple Dirk, which differed for vernalization response, increased as the strength of the response increased. At the four temperatures Triple Dirk D (Vrn 1 vrn 2) was not significantly different from normal Triple Dirk (Vrn 1 Vrn 2) but Triple Dirk B (vrn 1 Vrn 2) was significantly (P=0.01) later than normal Triple Dirk at each temperature. This indicates that the vrn 1 allele confers stronger vernalization response than vrn 2 over the range of temperatures (9–24°C). However, Triple Dirk C (vrn 1 vrn 2) failed to head after 120 days at each temperature indicating strong interaction between vrn 1 and vrn 2 with each other (and possibly the Triple Dirk back-ground) to give a much stronger vernalization response than predictions from additivity of their individual effects.The second set comprised the four Chinese Spring/Thatcher chromosome substitution lines CS/T 3B, 6B, 7B and 5D, plus Chinese Spring and Thatcher, and were grown in the unvernalized condition. CS/T 5D was similar in days to ear emergence as Chinese Spring at all four temperatures but the other three lines were earlier to ear emergence, particularly as the temperature increased. Days to ear emergence was fastest at 14°C in all lines, except CS/T 3B, in which it decreased progressively from 9 to 24°C.The third set of Chinese Spring and Thatcher and the homoeologous group 2 chromosomes of Thatcher substituted in Chinese Spring, the group which is considered to be involved in the control of photoperiod sensitivity. The three substitution lines responded differently to temperature compared with Chinese Spring and with each other, with chromosome 2D being the least, and chromosome 2B the most, responsive to temperature. 相似文献
18.
小麦粒重基因定位研究 总被引：20，自引：0，他引：20
本文以低粒重的多小穗品种"10阿"为被测材料,"中国春" 和"阿勃"两套单体系列为测验系,对粒重性状进行了基因定位研究.结果表明,被测材料"10阿"粒重低受5A、1B、2B、2D和7D等染色体上的隐性基因所控制。从其减小效应的程度来看,1B和2B染色体上的基因表现为强效。5A、6B、2D和7D染色体上的基因表现为弱效。 相似文献
19.
Synthesis of high and low pI α-amylase in germinating wheat grains and GA3-treated de-embryonated grains of Chinese Spring (CS) and its ditelosomic derivative (CS dit 6BS) were compared and related
to high pI α-amylase production in grains affected by late maturity α-amylase (LMA). In de-embryonated grains of CS dit 6BS
(lacking the long arm of chromosome 6B) treated with GA3, synthesis of high pI α-amylase isozymes controlled by Amy-1 genes on chromosomes 6A and 6D was dramatically reduced compared
to Chinese Spring. The results suggest the presence of a gene(s) on the long arm of chromosome 6B, which is (are) required
for GA-induced α-amylase synthesis in the aleurone. Similarly, in wheat grains affected by LMA, high pI α- Amy genes on the
group 6 chromosomes are activated apparently by a single gene, tentatively located on chromosome 6B. Both genes may be part
of the GA-induced amylase synthesis pathway in the aleurone. By contrast, synthesis of the high pI α-amylase isozymes in the
early stages of germination of CS dit 6BS grains was very similar to CS. This contrast between GA3-treated de-embryonated grains and germinating grains could be explained by control of α-amylase synthesis in scutellum in
the early stages of germination being different to that in GA3-treated aleurone.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
20.
Two series of progenies were developed from hybrids between octoploid (AABBDDRR) and tetraploid triticale ((AB)(AB)RR). One arose from the successive selfing of the F1s, while the second was established after one backcross of the F1 hybrids with the respective 8 × triticale parent. Altogether, 250 F3 and BC1F2 lines were developed, of which 112 were karyotyped in the F4/F5 or in BC1F3/BC1F4 generations using C-banding and SDS-PAGE. The 112 lines represented 61 different karyotypes, of which 39 appeared to be stabilized, having pairs of homologous wheat chromosomes only, while 22 karyotypes exhibited 1—3 heterologous pairs. The frequency of karyotypically stabilized lines originating from the series with one backcrossing was much higher (79.5 %) than those derived from the successive selfing of the F1 hybrids (51.7%). Six lines had the pure hexaploid triticale chromosome constitution. The frequency of disomic substitutions of D genome chromosomes for their homoeologous A and/or B genome chromosomes ranged from one to six per line with an average of 1.7. Except for 3B and 6B all possible D(A/B) substitutions were obtained. Chromosomes ID and 3D substituted for their homoeologues with the highest frequency, while the substitution of chromosome 4D for 4A or for 4B was the least frequent. D(R) substitutions were found in eight lines only. A complete set of 6x triticale lines was established in which chromosome ID was present in all possible combinations, i.e. single 1D(1A/1B/1R) disomic substitutions as well as disomic ID addition. 相似文献