Evidence map›Paper›PMID 37378747›Full record

ArticleMolecular biology reports2023

Development and validation of most efficient RNA isolation method from buffalo bull spermatozoa.

Rashi Vasisth, Ankita Gurao, Namita Kumari, Gautam Kumar, Anurag Kumar, Karpenahalli Ranganatha Sriranga, Mahesh Shivanand Dige, Manishi Mukesh, Rajeev Anand Kumar Aggarwal, Pawan Singh and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Rashi VasisthAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Ankita GuraoAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Namita KumariAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Gautam KumarAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Anurag KumarAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Karpenahalli Ranganatha SrirangaICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India.
Mahesh Shivanand DigeAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Manishi MukeshAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Rajeev Anand Kumar AggarwalAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India.
Pawan SinghICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India.
Ranjit Singh KatariaAnimal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana, 132001, India. katariaranji@yahoo.co.in.ORCID http://orcid.org/0000-0003-2845-7486
National Bureau of Animal Genetic Resources · INNational Dairy Research Institute · IN

Funding

Department of Biotechnology, Ministry of Science and Technology, India BT/PR30439/AAQ/1/743/ 2019
6 · The paper itself

Abstract

backgroundBeing highly fragmented and low in concentration, isolation of good quality RNA from sperm cells is a big challenge. Attempts have been made to evaluate various sperm RNA isolation methods from purified buffalo bull sperm cells.

methodsBoth, non-membrane and membrane-based methods have been evaluated for isolating RNA from Murrah buffalo sperms and compared for their respective efficacies. The traditional TRIzol, TRIzol-heat lysed (H-TRIzol) and cocktail of TCEP-RLT lysis buffer (Qiagen RNeasy mini kit)-TRIzol (C-TRIzol) based isopropanol isolation methods have been evaluated.

resultsH-TRIzol yielded best results among conventional methods. The combined T-RLT RNA isolation protocol yielded best quality and quantity compared to other membrane-based methods, due to high lytic property of cocktail of lysis reagents, necessary for complete breakdown of sperm membrane and RNA binding membrane for RNA isolation. Combined lysis performed by treatment with RLT-T and T-RLT differing in order of reagents used were also evaluated. T-RLT combination giving better results compared to RLT-T due to high gDNA contamination and membrane clogging in later protocol steps.

conclusionOverall, in terms of total RNA quantity and quality per million spermatozoa, the heat-lysed TRIzol method (H-TRIzol) performs best among RNA separation techniques employed and is also quite easy to perform. This comparative evaluation of sperm RNA isolation protocols can be useful in deciding the best protocol for isolation of good quality and high concentration sperm RNA from buffalo semen, for transcriptome and other downstream studies.

Indexed as

RNASemen PreservationAnimalsBuffaloesCryopreservationGuanidinesMalePhenolsSemenSpermatozoaGuanidinesPhenolsRNAtrizolBuffalo bullPurificationQuality checkRNA isolationSemenSpermatozoa

Identifiers

PMID37378747
OpenAlexW4382344252

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.