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Rzqust [24]
3 years ago
12

how do you think earths large temperature gradient affects the speed of its convection currents how would this speed change if e

arths core was cooler
Biology
1 answer:
dezoksy [38]3 years ago
7 0
A higher temperature gradient causes faster heat transfer, and thus faster convection currents. If the core were cooler, the temperature gradient would be lower, so the convection currents would likely slow down.
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Name a contractile protein in our body.
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Explanation:

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Compare and contrast Prophase and Telophase. what is different about DNA of the chromosomes in these phases. ( Max 5 Sentences )
shepuryov [24]

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The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.

1. The C. elegans embryo as a system to study cell division

The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.

Explanation:

4 0
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daser333 [38]

A

Explanation:

The genome of prokaryotes has no introns hence their mRNA does not need splicing like in eukaryotic cells. Also, because the genome of prokaryotes is not delimited from the cytoplasm by a nuclear membrane, ribosomes can attach to the elongating mRNA during transcription and begin translation. Therefore translation of mRNA occurs concurrently with transcription which cannot happen with eukaryotic cells.

In the nucleus of eukaryotic cells, transcription results to a nascent mRNA which is spliced into a mature mRNA.The mature mRNA has to travel outside the nucleus to the cytoplasm to be translated by ribosomes.

Learn More:

brainly.com/question/11655383

brainly.com/question/13276299

brainly.com/question/13551177

brainly.com/question/11515691

#LearnWithBrainly

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s2008m [1.1K]

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