scholarly journals Chromosome count, meiotic abnormalities and pollen sterility in Lahaul sweetvetch (Hedysarum astragaloides Benth. ex Baker, Fabaceae), an endemic and threatened species from India

2018 ◽  
Vol 77 (2) ◽  
pp. 203-208 ◽  
Author(s):  
Puneet Kumar ◽  
Pawan Kumar Rana ◽  
Vijay Kumar Singhal ◽  
Harminder Singh ◽  
Bhupendra Singh Kholia

Abstract Male meiotic studies were carried out on eight different accessions of Hedysarum astragaloides Benth. ex Baker (Fabaceae), an endemic and threatened species of northwest Himalaya, India. Although genetic factors such as meiosis, chromosome number, and ploidy level may be causative for the evolution, endemism, rare distribution or even extinction of the species, no detailed information exists. Keeping this in mind H. astragaloides has been studied cytologically. Male meiotic investigations revealed diploid level (2n=2x=14) for species and normal meiotic course in the accessions from the Manali Hills resulting in nearly 100% pollen fertility. However, the accessions scored from the Manimahesh Hills and Pangi Valley depicted inter-pollen mother cell transfer of chromatin material and structural heterozygosity for reciprocal translocations. Consequent upon these meiotic anomalies, some pollen sterility (21%) resulted. On account of this sweeping genetic outcome, the incidence of anomalies such as this in an endemic and threatened species warrants grave consideration. It is sensible to conclude that conservation measures should include the collection of germplasm from the localities where plants are meiotically stable with high gametic fertility, to ensure good germination and healthy plants for future use. Seeds from meiotically normal individuals should be given priority for inclusion in seed banks.

2005 ◽  
Vol 13 (11) ◽  
pp. 1205-1212 ◽  
Author(s):  
Julia Baptista ◽  
Elena Prigmore ◽  
Susan M Gribble ◽  
Patricia A Jacobs ◽  
Nigel P Carter ◽  
...  

Caryologia ◽  
2015 ◽  
Vol 68 (3) ◽  
pp. 246-253 ◽  
Author(s):  
Rohit Kumar ◽  
Pawan Kumar Rana ◽  
Himshikha ◽  
Dalvir Kaur ◽  
Maninder Kaur ◽  
...  

2013 ◽  
Vol 61 (1-4) ◽  
pp. 64-72 ◽  
Author(s):  
Firdose R. Kolar ◽  
Sandeep R. Pai ◽  
Ghansham B. Dixit

Meiotic cell division is a dynamic cellular process controlled by a large number of genes that act from premeiotic to postmeiotic mitosis. Mutation in these genes may cause anomalies that impair plant fertility. In this study, an attempt has therefore been made to understand the effects of ethyl methane sulfonate (EMS), sodium azide (SA) and gamma rays on the meiotic configuration of Delphinium malabaricum. The results demonstrated that the mutagens cause various types of cytological aberrations, such as univalents, chromatin bridges, laggards, fragments, stickiness and multinucleated cells. The maximum aberrations were found at higher doses/concentrations of the mutagens. The highest percentage of pollen mother cells showing abnormalities was induced by EMS followed by gamma rays and SA. The mutagen impact on chromosomal anomalies increased the frequency of pollen sterility.


1984 ◽  
Vol 26 (5) ◽  
pp. 499-505 ◽  
Author(s):  
P. Sateesh Kumar ◽  
N. C. Subrahmanyam ◽  
D. G. Faris

Cytological study of a hybrid between Cajanus cajan and Atylosia albicans revealed regular bivalent formation and disjunction. Nevertheless, high pollen sterility and low seed set were evident. An examination of pollen mother cells revealed variation in nucleolar number at telophase-I (four to eight) and at telophase-II (zero to four in daughter nuclei), although each genome contained two nucleolar organizers. Variation was also recorded for nucleolar size and distribution at telophase-II. Variation in nucleolar number and distribution are interpreted to have originated from pairing and recombination between nucleolar organizer chromosome(s) of one parental species with the nonnucleolar organizer chromosome(s) of the other. Size variation is attributed to nucleolar dominance. These results explain the high degree of pollen sterility in the hybrid in spite of normal meiosis, and also suggest that the karyotypes of C. cajan and A. albicans have differentiated through structural heterozygosity.Key words: Cajanus cajan, Atylosia albicans, nucleolar variation, structural heterozygosity, allosyndetic recombination.


1985 ◽  
Vol 16 (4) ◽  
pp. 260-266 ◽  
Author(s):  
Lee Ann Laraway

The purpose of this study was to determine whether there is a statistically significant difference between the auditory selective attention abilities of normal and cerebral-palsied individuals. Twenty-three cerebral-palsied and 23 normal subjects between the ages of 5 and 21 were asked to repeat a series of 30 items consisting of from 2 to 4 digits in the presence of intermittent white noise. Results of the study indicate that cerebral-palsied individuals perform significantly poorer than normal individuals when the stimulus is accompanied by noise. Noise was not a significant factor in the performance of the normal subjects regardless of age.


1992 ◽  
Vol 68 (04) ◽  
pp. 464-469 ◽  
Author(s):  
Y Fujimura ◽  
S Miyata ◽  
S Nishida ◽  
S Miura ◽  
M Kaneda ◽  
...  

SummaryWe have recently shown the existence of two distinct forms of botrocetin (one-chain and two-chain), and demonstrated that the two-chain species is approximately 30 times more active than the one-chain in promoting von Willebrand factor (vWF) binding to platelet glycoprotein (GP) Ib. The N-terminal sequence of two-chain botrocetin is highly homologous to sea-urchin Echinoidin and other Ca2+-dependent lectins (Fujimura et al., Biochemistry 1991; 30: 1957–64).Present data indicate that purified two-chain botrocetin binds to vWF from plasmas of patients with type IIA or IIB von Willebrand disease and its interaction is indistinguishable from that with vWF from normal individuals. However, an “activated complex” formed between botrocetin and IIB vWF expresses an enhanced biological activity for binding to GP Ib whereas the complex with IIA vWF has a decreased binding activity. Among several anti-vWF monoclonal antibodies (MoAbs) which inhibit ristocetin-induced platelet aggregation and/or vWF binding to GPIb, only two MoAbs (NMC-4 and RFF-VIII RAG:1) abolished direct binding between purified botrocetin and vWF. This suggests that they recognize an epitope(s) on the vWF molecule in close proximity to the botrocetin binding site.


1989 ◽  
Vol 61 (01) ◽  
pp. 111-116
Author(s):  
Sharron L Pfueller ◽  
Robyn A Bilston ◽  
Dana Logan ◽  
Rosemary David ◽  
Ian G Sloan ◽  
...  

SummaryReactivity of quinine- and quinidine-dependent antiplatelet antibodies has been compared in platelet-rich-plasma (PRP) from normal donors and from patients with von Willebrand’s disease (vWd). One quinine-dependent antibody (Q. Ab) caused platelet aggregation and [14C] serotonin release with only 7 of 12 normal donors, while another Q. Ab and a quinidine-dependent antibody (Qd. Ab) caused aggregation and release with all 12. Drug- dependent IgG binding and PF 3 availability induced by the antibodies were, however, comparable in all donors. Differences in responsiveness were associated with platelets and not plasma. vWd platelets showed normal drug-dependent IgG binding, but decreased aggregation and serotonin release to most drug- dependent antibodies. Responsiveness was not restored by purified vWf:Ag, but, in one case, was corrected by normal plasma or cryoprecipitate. Drug-dependent binding of the Q. Ab which caused variable responsiveness in normals was to the same platelet antigens (GPIb and GPIIIa) in both normal and vWd platelets and did not require plasma components. Reduced PF 3 availability was seen with some antibodies in some vWd patients. Plasma from two of these patients inhibited aggregation of normal platelets to Q. Ab and one of these inhibited aggregation to ADP. Antiplatelet antibodies were detected in these two plasmas by ELISA. Thus some Q. Ab produce different responses with platelets from different donors. In vWd, reduced responsiveness to Q.Ab and Qd. Ab may result from production of inhibitory antiplatelet antibodies.


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