Sources and inheritance of earliness in tropically adapted indeterminate common bean

Summary Nineteen early maturing, indeterminate common bean parents were crossed with a tester line of normal maturity. All parents, F₁ hybrids, F₂'s, and backcross generations were evaluated at CIAT-Palmira, Colombia. All 19F₁ populations flowered and matured almost as early as the respective early parent (mean of 61 vs 59 days). The F₂ populations were slightly less early (63 days), but were still earlier than the mean of the two parents (65 days). Additive effects for days to maturity were usually larger than dominance or interaction effects. Narrow sense heritability for days to flower and maturity were high (greater than 0.67), while heritabilities of absolute and relative duration of pod filling were low (0.17 to 0.50). Also, our data indicated that for each day of increase in earliness, yield potential will decrease 74 kg/ha.     

Genetics of resistance to ascochyta blight in chickpea (Cicer arietinum L.)

Summary Six chickpea lines resistant to Ascochyta rabiei (Pass.) Lab. were crossed to four susceptible cultivars. The hybrids were resistant in all the crosses except the crosses where resistant line BRG 8 was involved. Segregation pattern for diseases reaction in F₂, BCP₁, BCP₂ and F₃ generations in field and glasshouse conditions revealed that resistance to Ascochyta blight is under the control of a single dominant gene in EC 26446, PG 82-1, P 919, P 1252-1 and NEC 2451 while a recessive gene is responsible in BRG 8. Allelic tests indicated the presence of three independently segregating genes for resistance; one dominant gene in P 1215-1 and one in EC 26446 and PG 82-1, and a recessive one in BRG 8.Research paper No. 3600     

Location of genes for chlorophyll synthesis on specific arms of chromosomes in Triticum aestivum

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).     

Cytoplasmic male sterility,resistance to gall mite and mildew,and season of leafing out in black currants

Summary Cytoplasmic male sterility (cms) is described in the F₁ hybrids Ribes × carrierei (R. glutinosum albidum × R. nigrum) and R. sanguineum × R. nigrum. In backcrosses to R. nigrum, progenies with R. glutinosum cytoplasm were either all male sterile, or segregated for full male fertility (F) and complete (S) and partial (I) male sterility. Ratios of F:I+S suggested that two linked genes controlled cms, F plants being dominant for one (Rf ₁) and recessive for the other (Rf ₂).Segregation for cms in relation to three linded genes, Ce (resistance to the gall mite, Cecidophyopsis ribes), Sph ₃(resistance to American gooseberry mildew, Sphaerotheca mors-uvae) and Lf ₁(one of two dominant additive genes controlling early season leafing out) indicated that Rf ₁and Rf ₂were in this linkage group. The gene order and approximate crossover values appeared to be: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqef0uAJj3BZ9Mz0bYu% H52CGmvzYLMzaerbd9wDYLwzYbItLDharqqr1ngBPrgifHhDYfgasa% acOqpw0xe9v8qqaqFD0xXdHaVhbbf9v8qqaqFr0xc9pk0xbba9q8Wq% Ffea0-yr0RYxir-Jbba9q8aq0-yq-He9q8qqQ8frFve9Fve9Ff0dme% aabaqaciGacaGaamqadaabaeaafaaakeaacaWGdbGaamyzamaamaaa% baGaaiiiaiaacccacaGGWaGaaiOlaiaacgdacaGG0aGaaiiiaiaacc% caaaGaaiiiaiaacccacaGGGaGaamOuaiaadAgaliaaigdakmaamaaa% baGaaiiiaiaacccacaGGGaGaaiiiaiaaccdacaGGUaGaaiOmaiaacs% dacaGGGaGaaiiiaiaacccacaGGGaGaaiiiaaaacaWGsbGaamOzaSGa% aGOmaOWaaWaaaeaacaGGGaGaaiiiaiaacccacaGGGaGaaiiiaiaacc% cacaGGGaGaaiiiaiaacccaaaGaamitaiaadAgaliaaigdakmaamaaa% baGaaiiiaiaacccacaGGGaGaaiiiaiaacccacaGGGaGaaiiiaiaacc% cacaGGGaGaaiiiaiaacccacaGGGaaaaiaadofacaWGWbGaamiAaSGa% aG4maaaa!6E4D!\[Ce\underline { 0.14 } Rf1\underline { 0.24 } Rf2\underline { } Lf1\underline { } Sph3\]. Crossover values of 0.36 for Ce-Lf ₁, and 0.15 for Lf ₁-Sph ₃were estimated from the relative mean differences in season of leafing out between seedlings dominant and recessive for Ce and Sph ₃.It is suggested that competitive disadvantage of lf ₁-carrying gametes and/or zygotes at low temperatures may be implicated in the almost invariable deficit of plants dominant for the closely linked mildew resistance allele Sph ₃. Poor performance of lf ₁- (and possibly lf ₂-) carrying gametes and young zygotes during periods of low temperature at flowering might also account for the liability of some late season cultivars and selections to premature fruit drop (running off).     

“Ch型”谷子显性核不育的遗传及其应用研究（Setaria italica）

通过对“Ch型”谷子显性核不育的遗传研究,证实“Ch型”的不育性与“澳大利亚谷”的细胞质无关,其育性是受两对显性连锁基因Ms-和Rf-上位互作控制的。其中Ms是显性不育基因,Rf是显性上位基因,当二者共同存在时,显性上位基因能抑制显性不育基因的表达,从而使不育表现可育。这种由杂交而来,并能找到“恢复系”的显性核不     

Genetic control of fatty acid composition in seed oil of Sinapis alba L.

Summary Inheritance of fatty acid composition was studied in an F1 diallel cross in Sinapis alba. Crosses were made among accessions having contrasting amounts of oleic (C18:1) and erucic (C22:1) acid. Concentrations of oleic, linoleic (C18:2), eicosenoic (C20:1) and erucic (C22:1) acids were determined by gas-chromatography for each mating combination. Genetic analysis confirmed that the composition of the fatty acids was controlled mainly by the nuclear genes of the embryo. Additive gene action with partial dominance for the reducing alleles was noted for oleic and linoleic acids, while erucic acid showed an additive mode of inheritance with partial dominance for the enhancing alleles. Positive heterosis was demonstrated for eicosenoic acid content. Erucic acid content was strongly negatively correlated with oleic acid, suggesting a genetic interdependence between the two fatty acids. Broad-sense and narrow-sense heritability estimates for each of oleic, linoleic and erucic acids were very high, due to low between-plants non-genetic component of variance.Contribution No. 3662-E, 1992 series.     

The Inheritance of Aliphatic Glucosinolates in Brassica napus

The inheritance of aliphatic glucosinolates was studied in crosses between synthetic B. napus lines and oilseed rape cultivars. Six unlinked loci are described which determine the aliphatic glucosinolate profile of B. napus. One locus regulates the presence or absence of propyl glucosinolates, while another regulates the expression of pentyl glucosinolates. Two loci regulate the removal of the terminal H₃CS-group from the amino acid derivative to produce alkenyl glucosinolates as opposed to methylthioalkyl and methylsulphinylalkyl glucosinolates, regardless of the length of the alkyl chain. Likewise, another two loci regulate the hydroxylation of both butenyl and pentenyl glucosinolates. The functional alleles at one of the hydroxylation loci results in significantly more hydroxylation than those at the other locus. The large number of aliphatic glucosinolates which have been described in Brassica thus results from an interaction between genes which regulate side chain elongation and genes which modify the structure of the side chain, regardless of its length. The implications of this study for the biosynthesis of aliphatic glucosinolates, the origin of B. napus and the potential to manipulate the leaf and seed glucosinolate profile of oilseed rape are discussed.     

Mapping genes for deep-seeding tolerance in barley

Deep-seeding tolerance, the emergence of seedlings from deep seeded conditions, is involved in stand establishment in semi-arid regions, where the soil surface is too dry for seed germination. Genes determining deep-seeding tolerance in barley were mapped using two doubled haploid populations derived from the following crosses: Harrington × TR306 (H/T)and Step toe × Morex (S/M). Significant quantitative trait loci (QTLs) for deep-seeding tolerance were found in each population. Two QTL sex plained 40% of the phenotypic variation in the H/T population and one QTL (S/M) 8% of the total phenotypic variance. Multiple QTLs accounting for coleoptile length and first internode length were detected in both populations. In the H/T population, there were coincident QTLs for deep-seeding tolerance, coleoptile length and first internode length on the long arm of chromosome 5H. These QTLs correspond with previously reported QTLs for abscisic acid and gibberellic acid response. QTL coincidence may be due to the pleiotropic effects of alleles at a single locus. This information may be useful for breeding programs manipulating morphological and physiological traits in order to develop varieties for semi-arid regions. This revised version was published online in August 2006 with corrections to the Cover Date.     

Introgression of alleles of the isozymic locus glucosephosphate isomerase-2 (GPI-2) from the CC genome of Brassica carinata to the CC genome of Brassica alboglabra and their independent segregation from seed colour

A yellowish brown‐seeded Brassica alboglabra was resynthesized from a (B. alboglabra×Brassica carinata) ×B. alboglabra cross, followed by self‐pollination. The resynthesized B. alboglabra lost the allele of the isozymic locus glucosephosphate isomerase‐2 (GPI‐2) from natural B. alboglabra, which was replaced by an allele from the corresponding genome in B. carinata. A simple Mendelian segregation of these two alleles was observed in the F₂ population of a natural × resynthesized B. alboglabra cross. Furthermore, these two alleles segregated independently from the seed colour.     

Genetic analysis of presence and absence of lint and fuzz in cotton

Cotton fibre mutants that were fuzzless and/or lintless were crossed with each other and a normal genotype (fuzzy, linted) to produce F₂ and BC₁ generations. F₂ segregation ratios from the cross of fuzzless‐lintless × fuzzy‐linted, for fuzzy‐linted, fuzzless‐linted and fuzzless‐lintless were 45 : 15 : 4. From the cross of fuzzless‐lintless × fuzzy‐linted, the F₂ segregation ratios were 9 : 39 : 16 whereas the BC₁F₁ segregation ratios from the F₁ backcrossed to fuzzless‐lintless were 1 : 3 : 4. These data suggest that the presence or absence of lint and fuzz are controlled by the interaction of four gene loci on non‐homologous chromosomes. We designate these loci as N₁, N₂, Li₃ and Li₄, where N₁ N₁ confers the presence of fuzzy, N₂N₂ confers inhibition of fuzzy initiation and development, and duplicate gene pairs, Li₃Li₃ and Li₄Li₄, determine the presence of lint. Homozygosity for li₃li₃ and li₄li₄ might also inhibit fuzz from development. In other words, they were recessive epistatic to fuzz genes.