A revised map of chromosome 16 in Gossypium hirsutum

Genome ◽  
1987 ◽  
Vol 29 (6) ◽  
pp. 823-827 ◽  
Author(s):  
Margaret Y. Menzel ◽  
Kenneth L. Richmond ◽  
Brian J. Dougherty
Keyword(s):  
Linkage Group ◽  
Gossypium Hirsutum ◽  
Key Words ◽  
Direct Evidence ◽  
Marker Gene ◽  
Chromosome 15 ◽  
Chromosome 16 ◽  
Group Iii ◽  
The Right ◽  
Key Words Cotton

Four translocations involving chromosome 16 (H16) in cotton (T1R;16R 2770, T1R;16R 4672, T15L;16R 8-5Ga, and T15R;16R 2767) were tested against telosomes for chromosome 16 and the H16 marker gene red plant (R1). The telosome tests confirmed that bp-2770 and bp-4672 are in the long (=right) arm of chromosome 16 and showed that bp-8-5Ga and bp-2767 are also in the long arm of H16, rather than in the short (=left) arm as previously reported. The locations of the chromosome 15 (H15) bp's for 8-5Ga and 2767 are also revised. A telosome test showed that H15 bp-8-5Ga is in the long (=left) arm. Consequently, H15 bp-2767 is placed in the short (=right) arm of chromosome 15. Duplication deficiencies mono- or tri-segmental for H16 (verified cytologically) showed that R1 is in the right (R) arm 24 cM distal to bp-2767 and 10 cM distal to bp-8-5Ga. Recombination frequencies showed that R1 is 13 cM from bp-4672 and 15 cM from bp-2770 (not significantly different). However, both of the T1R;16R translocations yield negligible frequencies of duplication deficiencies and therefore offered no direct evidence as to whether their breakpoints are proximal or distal to R1. Previous estimates have placed both bp-2770 and bp-4672 43 cM from the centromere. Therefore the order must be as follows: (left)–centromere–bp-2767-bp-8-5Ga–R1–bp-4672/bp-2770 (right). Key words: cotton, Gossypium hirsutum, chromosome 16, translocations, linkage map, duplication-deficiences, red plant, linkage group III.

A revised map of chromosome 15 in Gossypium hirsutum

1986 ◽  
Vol 28 (2) ◽  
pp. 272-277 ◽  
Author(s):  
Margaret Y. Menzel ◽  
Kenneth L. Richmond
Keyword(s):  
Linkage Group ◽  
Gossypium Hirsutum ◽  
Marker Genes ◽  
Chromosome 15 ◽  
Linkage Maps ◽  
Leaf Veins ◽  
Group Ii ◽  
The Right

Three translocations involving chromosome 15 (H15) in cotton, T4R;15L 1040, T11L;15L 1058a, and T15R;20R SL15, were tested against the H15 marker genes okra leaf [Formula: see text] and veins fused (vf). The latter gene was also tested against T15L;16L 2767. Duplication deficiencies monosegmental for H15 (easily recognized by their narrow distorted bacteoles) showed that [Formula: see text] is in the right (R) arm distal to the SL15 breakpoint (bp-SL15) and cannot be distal to bp-1040 or bp-1058a in the left (L) arm. Recombination frequencies between the three bp's and [Formula: see text] showed that the order is (L) bp-1058a–bp-1040–centromere–bp-SL15–[Formula: see text]. [Formula: see text] is approximately 28 cM (centi-Morgan) from the centromere. The L and R arms of H15 defined by translocations correspond, respectively, to the long and short arms defined by telosomes. Duplication deficiencies monosegmental for H15 showed that vf is not distal to either the L arm or the R arm bp's in H15. Therefore vf and the genes Lg, s, and cr, which are closely linked to vf, cannot be located on H15 as had been assumed. "Linkage group II" thus contains genes located on two different chromosomes. We suggest retaining linkage group II for Lg and genes closely linked to it and designating the group of genes on H15 linked to [Formula: see text] as linkage group XIX.Key words: cotton, translocations, linkage maps, duplication–deficiencies, okra leaf, veins fused.

scholarly journals Correlation of the physical and genetic maps of the centromeric region of the right arm of linkage group III of Neurospora crassa.

Genetics ◽  
1994 ◽  
Vol 136 (4) ◽  
pp. 1297-1306
Author(s):  
C R Davis ◽  
R R Kempainen ◽  
M S Srodes ◽  
C R McClung
Keyword(s):  
Linkage Group ◽  
Neurospora Crassa ◽  
Fragment Length Polymorphism ◽  
Centromeric Region ◽  
Recombination Frequency ◽  
Genetic Maps ◽  
Polymorphism Analysis ◽  
Group Iii ◽  
Sib Selection ◽  
The Right

Abstract We have cloned three linked genes serine-1 (ser-1), proline-1 (pro-1) and acetate-2 (ace-2) that lie near the centromere on the right arm of linkage group III (LGIIIR) of Neurospora crassa. The ser-1 gene was cloned by sib selection. A chromosomal walk that spans 205 kilobases (kb) was initiated from ser-1. Complementation analysis with clones isolated during the walk allowed identification of the pro-1 and ace-2 genes. Restriction fragment length polymorphism analysis has confirmed the localization of ser-1, pro-1 and ace-2 to the centromeric region of LGIIIR. Genetically, we measured 1% recombination between ser-1 and pro-1 and 2% recombination between pro-1 and ace-2. Physical distances for these intervals were 114 kb from ser-1 to pro-1 and 36 kb from pro-1 to ace-2. Thus, for the pro-1 to ace-2 interval we calculate a physical/genetic correlation of 18 kb/map unit (mu) whereas, in the immediately adjacent, centromere-proximal interval from ser-1 to pro-1, we calculate 114 kb/mu. This provides evidence for a centromere effect, a decrease in recombination frequency as one approaches the centromere.

scholarly journals IDENTIFIKASI DAN UJI KAPASITAS REPRODUKSI PARASITOID TELUR ULAT PENGGEREK BUAH MERAH JAMBU PADA TANAMAN KAPAS

2020 ◽  
Vol 11 (3) ◽  
pp. 94
Author(s):  
DWI ADI SUNARTO ◽  
NURINDAH NURINDAH ◽  
SUJAK SUJAK
Keyword(s):  
Biological Control ◽  
Gossypium Hirsutum ◽  
Key Words ◽  
Biological Control Agent ◽  
Egg Parasitoid ◽  
Control Agent ◽  
Pectinophora Gossypiella ◽  
Control Actions ◽  
Key Words Cotton ◽  
Trichogrammatoidea Bactrae

<p>ABSTRAK<br />Pectinophora gossypiella merupakan salah satu hama utama<br />tanaman kapas yang menyerang dengan cara menggerek buah. Mulai<br />stadia larva kecil hingga pupa berada di dalam buah. Perilaku tersebut<br />menjadi salah satu sebab kurang efektifnya beberapa cara pengendalian P.<br />gossypiella dengan sasaran stadia larva. Untuk itu, peluang yang<br />diharapkan akan memberikan hasil pengendalian yang lebih baik adalah<br />sasaran pada stadia telur yaitu antara lain pemanfaatan parasitoid telur.<br />Dari hasil eksplorasi telah diperoleh parasitoid telur Trichogrammatidae<br />yang berasal dari pertanaman kapas di Lamongan dan Asembagus, Jawa<br />Timur. Penelitian ini bertujuan untuk mengidentifikasi spesies parasitoid<br />telur P. gossypiella dan kapasitas reproduksinya. Penelitian ini<br />dilaksanakan di Balai Penelitian Tanaman Tembakau dan Serat Malang<br />pada bulan Maret - Desember 2002. Hasil penelitian menunjukkan bahwa<br />parasitoid telur Trichogrammatidae yang muncul dari telur P. gossypiella<br />yang berasal dari kedua lokasi, berasal dari spesies yang sama dan berbeda<br />dengan spesies T. armigera yang memarasit telur H. armigera.<br />Berdasarkan kapasitas reproduksinya, Trichogrammatoidea bactrae N &amp; N<br />berpotensi sebagai agens hayati pengendali ulat penggerek buah kapas<br />merah jambu P. gossypiella.<br />Kata kunci : Kapas,  Gossypium  hirsutum,  hama,  Pectinophora<br />gossypiella,  parasitoid  telur,  Trichogrammatidae,  laju<br />pertumbuhan</p><p><br />ABSTRACT<br />Identification and reproduction capacity test of egg<br />parasitoid pink bollworm, Pectinophora gossypiella<br />Saunders on cotton<br />Pectinophora gossypiella is one of main pests of cotton. It attacks<br />the boll since small larvae until pupae and the insect is located in the boll.<br />This could be the reason why any control actions targeted to the larvae<br />were not effective. Therefore, the use of egg parasitoid to control the<br />bollworm population would be more promising. Exploration of the egg<br />parasitoid of the bollworm was done in Lamongan and Asembagus, East<br />Java. The parasitoids were considered as new locality report. This study<br />was to identify egg parasitoid of P. gossypiella and to study their<br />reproduction capacity. The study was conducted in Biological Control<br />Laboratory of IToFCRI Malang, March – December 2002. The study<br />included identification morphologically and biosystematically. The results<br />showed that Trichogrammatid emerged from P. gossypiella egg collected<br />from Asembagus (Trichogrammatoidea sp-A) and Lamongan (Trichogra-<br />mmatoidea sp-L) were the same species. Based on the reproduction<br />capacity of the parasitoids, Trichogrammatoidea bactrae N &amp; N were<br />potential as biological control agent for P. gossypiella.<br />Key words : Cotton,  Gossypium  hirsutum,  pest,  Pectinophora<br />gossypiella, egg parasitoid, Trichogrammatidae, intrinsic<br />rate</p>

A CROSSOVER SUPPRESSOR-ENHANCER SYSTEM IN THE MOSQUITO AEDES AEGYPTI

1971 ◽  
Vol 13 (3) ◽  
pp. 561-577 ◽  
Author(s):  
Satish C. Bhalla
Keyword(s):  
Linkage Group ◽  
Reciprocal Translocation ◽  
Paracentric Inversion ◽  
Chromosome 1 ◽  
Crossing Over ◽  
Linkage Groups ◽  
Group Iii ◽  
Partial Sterility ◽  
The Right ◽  
And Inversion

A small reciprocal translocation T(1;2)1 involving chromosomes 1 and 2 and a paracentric inversion In(1)3 on m chromosome (1) of A. aegypti interact to give peculiar but consistent crossover values. The system is termed COSES and is associated with partial sterility. In females it suppresses crossing over tremendously to the right of bz and enhances crossing over to its left. In the males it enhances crossing over to the right of m (only 3 crossover units away from bz) hut the region to its left remains unaffected. COSES also displays interchromosomal effects by enhancing crossing over in linkage group III. Cytological and genetic evidence for the presence of translocation and inversion are presented. All three pairs of chromosomes are correlated to the three linkage groups.

scholarly journals THE T6 TRANSLOCATION IN THE MOUSE: ITS USE IN TRISOMY MAPPING, CENTROMERE LOCALIZATION, AND CYTOLOGICAL IDENTIFICATION OF LINKAGE GROUP III

Genetics ◽  
1972 ◽  
Vol 71 (4) ◽  
pp. 621-632
Author(s):  
Eva M Eicher ◽  
Margaret C Green
Keyword(s):  
Linkage Group ◽  
The Other ◽  
Chromosome 15 ◽  
Chromosome 14 ◽  
Group Iii ◽  
Translocation Heterozygote ◽  
Chromosome Segments

ABSTRACT The occurrence of hairless piebald mice trisomic for the chromosome segments of the T6M chromosome has shown that the LG III loci hr and s are not located on T6M. The T6 breakpoint in LG III is therefore in the position hr—s—T6. T6M must carry the gene Fkl, which is located on the far side of the T6 breakpoint from hr in LG III.—T6 reduces recombination in the hr—s region.—Trisomy for the chromosome segments of the T6M chromosome appears to severely reduce viability.—The gene hr has been shown to lie between the centromere and the T6 breakpoint. The order of loci in LG III is therefore: centromere—hr—s—T6.—Equations are given for the relation between the frequency of adjacent-2 segregation and the frequency of recovery of complementation zygotes for the case in which the translocation heterozygote can form either quadrivalent or univalent-trivalent configurations at meiosis.—Linkage Group III is carried on chromosome 14. LG VI is the other linkage group involved in T6, and is carried on chromosome 15.

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). IX. Definition of linkage group III and further mapping of linkage groups I and II

1984 ◽  
Vol 26 (3) ◽  
pp. 253-257 ◽  
Author(s):  
R. H. Gooding
Keyword(s):  
Linkage Group ◽  
Aldehyde Oxidase ◽  
Glossina Morsitans Morsitans ◽  
Linkage Groups ◽  
Glossina Morsitans ◽  
Malic Dehydrogenase ◽  
Group Iii ◽  
Glycerophosphate Dehydrogenase ◽  
Group I ◽  
The Right

In Glossina morsitans morsitans Westwood, linkage group III is defined as the autosome carrying the locus Mdh (malic dehydrogenase), the only locus so far identified in this linkage group. The locus αGpd.2 (α-glycerophosphate dehydrogenase) was located 45 map units (MU) to the left of Xo (xanthine oxidase) and the loci Est.1 and Est.2 (loci for two esterases found in the thorax) were mapped approximately 5–10 MU to the right of Ao (aldehyde oxidase) in linkage group II. The location of G6pd (glucose-6-phosphate dehydrogenase) has been confirmed to be approximately 37 MU to the left of oc (ocra body color) in linkage group I and it was shown that this region of the X chromosome does not involve the large paracentric inversion found in the Handeni line. A genetic map for 12 loci in the three linkage groups found in G. m. morsitans is presented.Key words: Diptera, Glossina, mapping, inversion, isozymes.

scholarly journals COMPLEMENTATION ANALYSIS OF LINKED CIRCADIAN CLOCK MUTANTS OF NEUROSPORA CRASSA

Genetics ◽  
1976 ◽  
Vol 82 (1) ◽  
pp. 9-17 ◽  
Author(s):  
Jerry F Feldman ◽  
Marian N Hoyle
Keyword(s):  
Linkage Group ◽  
Circadian Clock ◽  
Neurospora Crassa ◽  
Period Length ◽  
Complementation Analysis ◽  
Wild Type ◽  
The Right

ABSTRACT A fourth mutant of Neurospora crassa, designated frq-4, has been isolated in which the period length of the circadian conidiation rhythm is shortened to 19.3 ± 0.3 hours. This mutant is tightly linked to the three previously isolated frq mutants, and all four map to the right arm of linkage group VII about 10 map units from the centromere. Complementation tests suggest, but do not prove, that all four mutations are allelic, since each of the four mutants is co-dominant with the frq  + allele—i.e., heterokaryons have period lengths intermediate between the mutant and wild-type—and since heterokaryons between pairs of mutants also have period lengths intermediate between those of the two mutants.

SEX AND CROSSING OVER IN LINKAGE GROUP III OF TRIBOLIUM CASTANEUM

1977 ◽  
Vol 19 (2) ◽  
pp. 259-263 ◽  
Author(s):  
Alexander Sokoloff
Keyword(s):  
Sex Differences ◽  
Linkage Group ◽  
Tribolium Castaneum ◽  
Relative Position ◽  
Genetic Background ◽  
Crossing Over ◽  
Group Iii ◽  
The Third ◽  
Main Factors ◽  
Coleoptera Tenebrionidae

The relative position of the genes black (b), light ocular diaphragm (lod) and aureate (au) for the third linkage group of T. castaneum (Herbst) (Coleoptera, Tenebrionidae) has been determined as b – lod – au. The distances between the various genes vary, depending on the cross. The b++/+ lod au ♂ × + lod au/+ lod au ♀ crosses give the following recombination values: au – lod = 18.32 ± 1.21%; b – lod = 21.05 ± 1.51% and b – au = 37.43 ± 1.27%. The reciprocal crosses give au – lod = 27.67 ± 1.62%; b – lod = 13.97 ± 1.26% and b – au = 39.79 ± 1.78%. For the larger distances encompassed in the b – au region the recombination values in the two sexes were not significantly different. For the shorter b – lod region the recombination values were significantly larger in the females than in the males, while for the adjacent lod – au region the opposite was true. On the basis of the current literature it would appear that the main factors contributing to these sex differences in recombination are the modifiers which are different in the genetic background of the two sexes.

Inhibition of cardiac vagal component of baroreflex by group III and IV afferents

1991 ◽  
Vol 260 (3) ◽  
pp. H730-H734 ◽  
Author(s):  
P. N. McWilliam ◽  
T. Yang
Keyword(s):  
Peroneal Nerve ◽  
Baroreceptor Reflex ◽  
Interval Prolongation ◽  
Group Iii ◽  
Control Value ◽  
Pressure Elevation ◽  
Group I ◽  
Afferent Fibers ◽  
The Difference ◽  
The Right

The action of electrically evoked activity in somatic afferent fibers on the sensitivity of the baroreceptor reflex was examined in decerebrate cats. The sensitivity of the reflex was expressed as the difference between the maximum prolongation of R-R interval in response to carotid sinus pressure elevation and the mean of 10 R-R intervals immediately before pressure elevation. The control value of R-R interval prolongation was 192 +/- 50 ms. Stimulation (10 Hz) of group I and II fibers of the right peroneal nerve (evoked volleys recorded from the sciatic nerve) had no effect on R-R interval prolongation (171 +/- 45 ms). Recruitment of group III fibers (10 Hz) conducting at 23.6 +/- 0.65 m/s reduced the prolongation of R-R interval to 52 +/- 14 ms. Recruitment of group IV fibers (10 Hz) conducting less than 2.5 m/s further reduced the prolongation of R-R interval to 1.0 +/- 8.0 ms. It is concluded that the inhibition of the cardiac vagal component of the baroreceptor reflex produced by electrical stimulation of the peroneal nerve is mediated by afferent fibers of groups III and IV.

Direct evidence for the contributive role of the right inferior fronto-occipital fasciculus in non-verbal semantic cognition

2016 ◽  
Vol 222 (4) ◽  
pp. 1597-1610 ◽  
Author(s):  
Guillaume Herbet ◽  
Sylvie Moritz-Gasser ◽  
Hugues Duffau
Keyword(s):  
Direct Evidence ◽  
Semantic Cognition ◽  
The Right
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