In vitro interspecific fertilization, embryo development and formation of hybrid seedlings between Gossypium hirsutum and G. arboreum

Euphytica ◽  
1992 ◽  
Vol 60 (2) ◽  
pp. 79-88 ◽  
Author(s):  
Chengzhi Liu ◽  
Jizhong Shun ◽  
Jinglan Liu
Keyword(s):  
Gossypium Hirsutum ◽  
Embryo Development

Induction of embryo development and fixation of partial interspecific lines after pollination of F1 cotton interspecific hybrids (Gossypium barbadense × Gossypium hirsutum) with pollen from Hibiscus cannabinus

2005 ◽  
Vol 56 (10) ◽  
pp. 1101 ◽  
Author(s):  
A. G. Mavromatis ◽  
S. K. Kantartzi ◽  
D. N. Vlachostergios ◽  
I. N. Xynias ◽  
G. N. Skarakis ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Gossypium Hirsutum ◽  
Embryo Development ◽  
Interspecific Hybrids ◽  
Morphological Traits ◽  
Gossypium Barbadense ◽  
Ovule Culture ◽  
Hibiscus Cannabinus ◽  
Egg Cell

The possibility of inducing embryo development after pollination of F1 interspecific cotton hybrids (Gossypium barbadense × Gossypium hirsutum) and their reciprocals with pollen from Hibiscus cannabinus was investigated. For this, flowers of F1 plants from 4 G. barbadense × G. hirsutum interspecific hybrids (B403 × Acala Sindos, Carnak × 4S, B403 × Coker 310, and Carnak × Acala Sindos) and their reciprocals grown in the field were pollinated with pollen from Hibiscus cannabinus. From the 443 pollinated flowers, 276 were left on the plant to grow naturally, and 167 were collected 5 days after pollination. Young ovules from the collected buds were cultured in vitro for embryo development. It was observed that, from the buds left to grow naturally on the mother plant, 21 bolls reached maturity. The mature bolls originated only from the 4 G. barbadense × G. hirsutum hybrids and contained 82 mature seeds. Finally, 38 plants (Pa0) were produced. From the in-ovule culture method, 10 young embryos were isolated from both G. barbadense × G. hirsutum and G. hirsutum × G. barbadense hybrids and finally 3 plants were produced. The plants produced from both approaches originated only from the G. barbadense × G. hirsutum hybrids. These plants exhibited morphological traits from both cotton species and they were partially fertile. No signs of H. cannabinus morphological traits were observed in the plants produced. Root-tip chromosome counts revealed that chromosome number among cells of the Pa0 plants ranged from 27 to 42 and the difference in chromosome number observed among cells of the same plant ranged from 1 to 3. The chromosome number, however, was increased progressively from generation to generation and in Pa3 it ranged from 46 to 52. Plants with 52 chromosomes were identified even from the Pa1 generation. In addition, flow cytometric analysis indicated that the parental plants had a similar DNA profile to the F1 and F2 interspecific hybrids but a different one from the Pa0 plants. Thus, alien pollination of cotton flowers from interspecific (G. barbadense × G. hirsutum and reciprocals) hybrids with pollen from H. cannabinus most likely induced parthenogenetic (Pa) egg cell development which, after a progressive chromosome increase, produced fully fertile plants with most of the cells at the tetraploid or near-tetraploid level. It was concluded that a combination of the in situ boll development with an optimised in vitro ovule culture technique could establish the ‘cannabinus method’ in cotton, as a method for the production of genotype-independent partial interspecific lines.

scholarly journals Calcium Carbonate Nanoparticles—Toxicity and Effect of In Ovo Inoculation on Chicken Embryo Development, Broiler Performance and Bone Status

Animals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 932
Author(s):  
Arkadiusz Matuszewski ◽  
Monika Łukasiewicz ◽  
Jan Niemiec ◽  
Maciej Kamaszewski ◽  
Sławomir Jaworski ◽  
...  
Keyword(s):  
Calcium Carbonate ◽  
Embryo Development ◽  
Bone Quality ◽  
Chicken Embryo ◽  
Broiler Chickens ◽  
Selection Procedure ◽  
High Specificity ◽  
Control Group ◽  
In Ovo

The use of intensive selection procedure in modern broiler chicken lines has led to the development of several skeletal disorders in broiler chickens. Therefore, current research is focused on methods to improve the bone quality in birds. In ovo technology, using nanoparticles with a high specificity to bones, is a potential approach. The present study aimed to evaluate the effect of in ovo inoculation (IOI) of calcium carbonate nanoparticles (CCN) on chicken embryo development, health status, bone characteristics, and on broiler production results and bone quality. After assessing in vitro cell viability, the IOI procedure was performed with an injection of 500 μg/mL CCN. The control group was not inoculated with CCN. Hatchability, weight, and selected bone and serum parameters were measured in embryos. Part of hatchlings were reared under standard conditions until 42 days, and production results, meat quality, and bone quality of broilers were determined. CCN did not show cytotoxicity to cells and chicken embryo and positively influenced bone parameters of the embryos and of broilers later (calcification) without negatively affecting the production results. Thus, the IOI of CCN could modify the molecular responses at the stage of embryogenesis, resulting in better mineralization, and could provide a sustained effect, thereby improving bone quality in adult birds.

scholarly journals Single cell RNA-seq reveals genes vital to in vitro fertilized embryos and parthenotes in pigs

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Zhi-Qiang Du ◽  
Hao Liang ◽  
Xiao-Man Liu ◽  
Yun-Hua Liu ◽  
Chonglong Wang ◽  
...  
Keyword(s):  
Embryo Development ◽  
Gene Networks ◽  
Regulatory Networks ◽  
Rna Binding ◽  
Expression Patterns ◽  
Early Embryo ◽  
Specific Factor ◽  
Early Embryos ◽  
Genome Activation

AbstractSuccessful early embryo development requires the correct reprogramming and configuration of gene networks by the timely and faithful execution of zygotic genome activation (ZGA). However, the regulatory principle of molecular elements and circuits fundamental to embryo development remains largely obscure. Here, we profiled the transcriptomes of single zygotes and blastomeres, obtained from in vitro fertilized (IVF) or parthenogenetically activated (PA) porcine early embryos (1- to 8-cell), focusing on the gene expression dynamics and regulatory networks associated with maternal-to-zygote transition (MZT) (mainly maternal RNA clearance and ZGA). We found that minor and major ZGAs occur at 1-cell and 4-cell stages for both IVF and PA embryos, respectively. Maternal RNAs gradually decay from 1- to 8-cell embryos. Top abundantly expressed genes (CDV3, PCNA, CDR1, YWHAE, DNMT1, IGF2BP3, ARMC1, BTG4, UHRF2 and gametocyte-specific factor 1-like) in both IVF and PA early embryos identified are of vital roles for embryo development. Differentially expressed genes within IVF groups are different from that within PA groups, indicating bi-parental and maternal-only embryos have specific sets of mRNAs distinctly decayed and activated. Pathways enriched from DEGs showed that RNA associated pathways (RNA binding, processing, transport and degradation) could be important. Moreover, mitochondrial RNAs are found to be actively transcribed, showing dynamic expression patterns, and for DNA/H3K4 methylation and transcription factors as well. Taken together, our findings provide an important resource to investigate further the epigenetic and genome regulation of MZT events in early embryos of pigs.

scholarly journals Analysis of Morphokinetic Parameters of Feline Embryos Using a Time-Lapse System

Animals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 748
Author(s):  
Joanna Kochan ◽  
Agnieszka Nowak ◽  
Barbara Kij ◽  
Sylwia Prochowska ◽  
Wojciech Niżański
Keyword(s):  
Embryo Development ◽  
Embryo Quality ◽  
Time Lapse ◽  
Blastocyst Stage ◽  
Cavity Formation ◽  
Non Invasive ◽  
Morphokinetic Parameters ◽  
Morphological Defects ◽  
Development In Vitro

The aim of this study was to analyze the morphokinetic parameters of feline embryos using a time lapse system. Oocytes matured in vitro were fertilized (IVF) and in vitro cultured in a time lapse-system (Primo Vision®, Gothenburg, Sweden). The first cell division of embryos occurred between 17 h post insemination (hpi) and 38 hpi, with the highest proportion of embryos (46%) cleaving between 21 and 24 hpi. The timing of the first cleavage significantly affected further embryo development, with the highest development occurring in embryos that cleaved at 21–22 hpi. Embryos that cleaved very early (17–18 hpi) developed poorly to the blastocyst stage (2%) and none of the embryos that cleaved later than 27 hpi were able to reach the blastocyst stage. Morphological defects were observed in 48% of the embryos. There were no statistically significant differences between the timing intervals of the first cleavage division and the frequency of morphological defects in embryos. Multiple (MUL) morphological defects were detected in more than half (56%) of the abnormal embryos. The most frequent single morphological defects were cytoplasmic fragmentation (FR) (8%) and blastomere asymmetry (AS) (6%). Direct cleavage (DC) from 1–3 or 3–5 blastomeres, reverse cleavage (RC) and vacuoles were rarely observed (2–3%). The timing of blastocyst cavity formation is a very good indicator of embryo quality. In our study, blastocyst cavity formation occurred between 127–167 hpi, with the highest frequency of hatching observed in blastocysts that cavitated between 142–150 hpi. Blastocysts in which cavitation began after 161 h did not hatch. In conclusion, the timing of the first and second cleavage divisions, the timing of blastocyst cavity formation and morphological anomalies can all be used as early and non-invasive indicators of cat embryo development in vitro.

Serial analysis of gene expression (SAGE) during porcine embryo development

2004 ◽  
Vol 16 (2) ◽  
pp. 87 ◽  
Author(s):  
Le Ann Blomberg ◽  
Kurt A. Zuelke
Keyword(s):  
Gene Expression ◽  
Functional Genomics ◽  
Embryo Development ◽  
Molecular Mechanisms ◽  
Physiological Role ◽  
Transgenic Animals ◽  
Specific Gene ◽  
Research Strategies

Functional genomics provides a powerful means for delving into the molecular mechanisms involved in pre-implantation development of porcine embryos. High rates of embryonic mortality (30%), following either natural mating or artificial insemination, emphasise the need to improve the efficiency of reproduction in the pig. The poor success rate of live offspring from in vitro-manipulated pig embryos also hampers efforts to generate transgenic animals for biotechnology applications. Previous analysis of differential gene expression has demonstrated stage-specific gene expression for in vivo-derived embryos and altered gene expression for in vitro-derived embryos. However, the methods used to date examine relatively few genes simultaneously and, thus, provide an incomplete glimpse of the physiological role of these genes during embryogenesis. The present review will focus on two aspects of applying functional genomics research strategies for analysing the expression of genes during elongation of pig embryos between gestational day (D) 11 and D12. First, we compare and contrast current methodologies that are being used for gene discovery and expression analysis during pig embryo development. Second, we establish a paradigm for applying serial analysis of gene expression as a functional genomics tool to obtain preliminary information essential for discovering the physiological mechanisms by which distinct embryonic phenotypes are derived.

scholarly journals Peroxidized mineral oil increases the oxidant status of culture media and inhibits in vitro porcine embryo development

2017 ◽  
Vol 103 ◽  
pp. 17-23 ◽  
Author(s):  
C.A. Martinez ◽  
A. Nohalez ◽  
J.J. Ceron ◽  
C.P. Rubio ◽  
J. Roca ◽  
...  
Keyword(s):  
Embryo Development ◽  
Culture Media ◽  
Mineral Oil ◽  
Porcine Embryo ◽  
Oxidant Status

In Vitro Regeneration of Four Commercial Cotton Cultivars (Gossypium hirsutum L.) Grown in Xinjiang, China

2008 ◽  
Vol 34 (8) ◽  
pp. 1374-1380
Author(s):  
Tian-Zi CHEN ◽  
Shen-Jie WU ◽  
Fei-Fei LI ◽  
Wang-Zhen GUO ◽  
Tian-Zhen ZHANG
Keyword(s):  
Gossypium Hirsutum ◽  
In Vitro Regeneration ◽  
Gossypium Hirsutum L
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